The DOI matches its Crossref record; 132 of the 132 references it cites were found in a registry or an index.
Ynamides: A Modern Functional Group for the New Millennium
Open accessAbstract
ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTYnamides: A Modern Functional Group for the New MillenniumKyle A. DeKorver†, Hongyan Li†, Andrew G. Lohse†, Ryuji Hayashi†, Zhenjie Lu†, Yu Zhang*‡, and Richard P. Hsung*†View Author Information Division of Pharmaceutical Sciences and Department of Chemistry, University of Wisconsin, Madison, Wisconsin 53705, and Discovery Research, Dow AgroSciences LLC, Indianapolis, Indiana 46268* To whom correspondence should be addressed. E-mail: [email protected] or [email protected]†University of Wisconsin.‡Dow AgroSciences LLC.Cite this: Chem. Rev. 2010, 110, 9, 5064–5106Publication Date (Web):April 29, 2010Publication History Received5 January 2010Published online29 April 2010Published inissue 8 September 2010https://pubs.acs.org/doi/10.1021/cr100003shttps://doi.org/10.1021/cr100003sreview-articleACS PublicationsCopyright © 2010 American Chemical SocietyRequest reuse permissionsArticle Views17304Altmetric-Citations782LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Addition reactions,Amides,Cyclization,Hydrocarbons,Mixtures Get e-Alerts
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Klapars, A., Antilla, J. C., Huang, X., & Buchwald, S. L. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016226z · Cited by 1,021
A General and Efficient Copper Catalyst for the Amidation of Aryl Halides
Klapars, A., Huang, X., & Buchwald, S. L. (2002) · Journal of the American Chemical Society · doi:10.1021/ja0260465 · Cited by 851
Ruthenium-Catalyzed Azide−Alkyne Cycloaddition: Scope and Mechanism
Boren, B. C., Narayan, S., Rasmussen, L. K., Zhang, L., Zhao, H., Lin, Z., Jia, G., & Fokin, V. V. (2008) · Journal of the American Chemical Society · doi:10.1021/ja0749993 · Cited by 829
Bae, I., Han, H., & Chang, S. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0432968 · Cited by 479
Copper-Catalyzed Aerobic Oxidative Amidation of Terminal Alkynes: Efficient Synthesis of Ynamides
Hamada, T., Ye, X., & Stahl, S. S. (2008) · Journal of the American Chemical Society · doi:10.1021/ja077406x · Cited by 476
Copper-Catalyzed Hydrative Amide Synthesis with Terminal Alkyne, Sulfonyl Azide, and Water
Cho, S. H., Yoo, E. J., Bae, I., & Chang, S. (2005) · Journal of the American Chemical Society · doi:10.1021/ja056399e · Cited by 447
Direct Synthesis of Pyridine Derivatives
Movassaghi, M., Hill, M. D., & Ahmad, O. (2007) · Journal of the American Chemical Society · doi:10.1021/ja073912a · Cited by 383
Zhang, Y., Hsung, R. P., Tracey, M. R., Kurtz, K. C. M., & Vera, E. L. (2004) · Organic Letters · doi:10.1021/ol049827e · Cited by 327
Self-citationRecent advances in the chemistry of ynamines and ynamides
Zificsak, C. A., Mulder, J. A., Hsung, R. P., Rameshkumar, C., & Wei, L.-L. (2001) · Tetrahedron · doi:10.1016/s0040-4020(01)00681-0 · Cited by 303
Self-citationPractical Synthesis of Amides from In Situ Generated Copper(I) Acetylides and Sulfonyl Azides
Cassidy, M. P., Raushel, J., & Fokin, V. V. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200503805 · Cited by 282
Tanaka, K., Takeishi, K., & Noguchi, K. (2006) · Journal of the American Chemical Society · doi:10.1021/ja060348f · Cited by 247
Ynamine: A versatile tool in organic synthesis
Ficini, J. (1976) · Tetrahedron · doi:10.1016/0040-4020(76)85200-3 · Cited by 235
Yoo, E. J., Ahlquist, M., Bae, I., Sharpless, K. B., Fokin, V. V., & Chang, S. (2008) · The Journal of Organic Chemistry · doi:10.1021/jo800733p · Cited by 230
Frederick, M. O., Mulder, J. A., Tracey, M. R., Hsung, R. P., Huang, J., Kurtz, K. C. M., Shen, L., & Douglas, C. J. (2003) · Journal of the American Chemical Society · doi:10.1021/ja021304j · Cited by 227
Self-citationAlkynyliodonium salts in organic synthesis
Zhdankin, V. V., & Stang, P. J. (1998) · Tetrahedron · doi:10.1016/s0040-4020(98)00410-4 · Cited by 225
Witulski, B., & Alayrac, C. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020902)41:17<3281::aid-anie3281>3.0.co;2-g · Cited by 214
Coste, A., Karthikeyan, G., Couty, F., & Evano, G. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200901099 · Cited by 211
Zhang, X., Zhang, Y., Huang, J., Hsung, R. P., Kurtz, K. C. M., Oppenheimer, J., Petersen, M. E., Sagamanova, I. K., Shen, L., & Tracey, M. R. (2006) · The Journal of Organic Chemistry · doi:10.1021/jo060230h · Cited by 208
Self-citationZhang, Y., Hsung, R. P., Zhang, X., Huang, J., Slafer, B. W., & Davis, A. (2005) · Organic Letters · doi:10.1021/ol0473391 · Cited by 196
Self-citationBuzas, A., & Gagosz, F. (2006) · Organic Letters · doi:10.1021/ol053100o · Cited by 195
A unique approach to aldol products for the creation of all-carbon quaternary stereocentres
Das, J. P., Chechik, H., & Marek, I. (2009) · Nature Chemistry · doi:10.1038/nchem.131 · Cited by 186
Dunetz, J. R., & Danheiser, R. L. (2003) · Organic Letters · doi:10.1021/ol035647d · Cited by 186
Dunetz, J. R., & Danheiser, R. L. (2005) · Journal of the American Chemical Society · doi:10.1021/ja051180l · Cited by 184
Frederick, M. O., Mulder, J. A., Tracey, M. R., Hsung, R. P., Huang, J., Kurtz, K. C. M., Shen, L., & Douglas, C. J. (2003) · ChemInform · doi:10.1002/chin.200327046 · Cited by 184
Self-citationRuthenium‐Catalyzed Cycloaddition of Nitrile Oxides and Alkynes: Practical Synthesis of Isoxazoles
Grecian, S., & Fokin, V. V. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200801920 · Cited by 180
Diastereoselective Gold‐Catalyzed Cycloisomerizations of Ene‐Ynamides
Couty, S., Meyer, C., & Cossy, J. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200602270 · Cited by 174
Copper‐Catalyzed Reaction Cascade: Direct Conversion of Alkynes into N‐Sulfonylazetidin‐2‐imines
Whiting, M., & Fokin, V. V. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200503936 · Cited by 171
Witulski, B., & Stengel, T. (1998) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19980302)37:4<489::aid-anie489>3.0.co;2-n · Cited by 167
Couty, S., Liégault, B., Meyer, C., & Cossy, J. (2004) · Organic Letters · doi:10.1021/ol049302m · Cited by 164
Witulski, B., & Stengel, T. (1999) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19990816)38:16<2426::aid-anie2426>3.0.co;2-y · Cited by 160
Zhang, X., Zhang, Y., Huang, J. Q., Hsung, R. P., Kurtz, K. C. M., Oppenheimer, J., Petersen, M. E., Sagamanova, I. K., Shen, L., & Tracey, M. R. (2006) · ChemInform · doi:10.1002/chin.200643041 · Cited by 157
Self-citationKramer, S., Dooleweerdt, K., Lindhardt, A. T., Rottländer, M., & Skrydstrup, T. (2009) · Organic Letters · doi:10.1021/ol901565p · Cited by 155
Gourdet, B., & Lam, H. W. (2009) · Journal of the American Chemical Society · doi:10.1021/ja900946h · Cited by 152
Hashmi, A. S. K., Rudolph, M., Bats, J. W., Frey, W. U., Röminger, F., & Oeser, T. (2008) · Chemistry - A European Journal · doi:10.1002/chem.200800210 · Cited by 150
Egi, M., Yamaguchi, Y., Fujiwara, N., & Akai, S. (2008) · Organic Letters · doi:10.1021/ol800596c · Cited by 145
A Ring-Closing Yne-Carbonyl Metathesis of Ynamides
Kurtz, K. C. M., Hsung, R. P., & Zhang, Y. (2005) · Organic Letters · doi:10.1021/ol052487s · Cited by 145
Self-citationSynthesis of Functionalized Oxazolones by a Sequence of Cu(II)- and Au(I)-Catalyzed Transformations
Istrate, F. M., Buzas, A. K., Jurberg, I. D., Odabachian, Y., & Gagosz, F. (2008) · Organic Letters · doi:10.1021/ol703077g · Cited by 143
Platinum Dichloride-Catalyzed Cycloisomerization of Ene-ynamides
Marion, F., Coulomb, J., Courillon, C., Fensterbank, L., & Malacrìa, M. (2004) · Organic Letters · doi:10.1021/ol049530g · Cited by 141
Witulski, B., & Stengel, T. (1999) · PubMed · Cited by 140
Fukudome, Y., Naito, H., Hata, T., & Urabe, H. (2008) · Journal of the American Chemical Society · doi:10.1021/ja078163b · Cited by 139
Huang, J. Q., Xiong, H., Hsung, R. P., Rameshkumar, C., Mulder, J. A., & Grebe, T. P. (2002) · Organic Letters · doi:10.1021/ol020097p · Cited by 134
Self-citationMulder, J. A., Kurtz, K. C. M., Hsung, R. P., Coverdale, H. A., Frederick, M. O., Shen, L., & Zificsak, C. A. (2003) · Organic Letters · doi:10.1021/ol0300266 · Cited by 132
Self-citationPalladium‐Catalyzed Synthesis of 2‐Aminoindoles by a Heteroanulation Reaction
Witulski, B., Alayrac, C., & Tevzadze‐Saeftel, L. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200351977 · Cited by 129
One-Pot Synthesis of Metalated Pyridines from Two Acetylenes, a Nitrile, and a Titanium(II) Alkoxide
Tanaka, R., Yuza, A., Watai, Y., Suzuki, D., Takayama, Y., Sato, F., & Urabe, H. (2005) · Journal of the American Chemical Society · doi:10.1021/ja050261e · Cited by 127
Gold-Catalyzed Cyclization of N-Alkynyl Carbamates
Hashmi, A. S. K., Salathé, R., & Frey, W. U. (2007) · Synlett · doi:10.1055/s-2007-982562 · Cited by 126
Efficient preparations of novel ynamides and allenamides
Wei, L., Mulder, J. A., Xiong, H., Zificsak, C. A., Douglas, C. J., & Hsung, R. P. (2001) · Tetrahedron · doi:10.1016/s0040-4020(00)01014-0 · Cited by 122
Self-citationSynthesis of Cyclic Dienamide Using Ruthenium-Catalyzed Ring-Closing Metathesis of Ene-Ynamide
Saito, N., Sato, Y., & Mori, M. (2002) · Organic Letters · doi:10.1021/ol017298y · Cited by 120
Couty, S., Liégault, B., Meyer, C., & Cossy, J. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.089 · Cited by 118
The First Stereoselective Ficini−Claisen Rearrangement Using Chiral Ynamides
Mulder, J. A., Hsung, R. P., Frederick, M. O., Tracey, M. R., & Zificsak, C. A. (2002) · Organic Letters · doi:10.1021/ol020037j · Cited by 117
Self-citationSaucy, G., & Marbet, R. (1967) · Helvetica Chimica Acta · doi:10.1002/hlca.19670500423 · Cited by 112
Feldman, K. S., Bruendl, M. M., Schildknegt, K., & Bohnstedt, A. C. (1996) · The Journal of Organic Chemistry · doi:10.1021/jo9605814 · Cited by 110
Stereochemical Control of Both C−C and C−N Axial Chirality in the Synthesis of Chiral N,O-Biaryls
Oppenheimer, J., Hsung, R. P., Figueroa, R., & Johnson, W. L. (2007) · Organic Letters · doi:10.1021/ol701692m · Cited by 108
Self-citationSynthesis of Carbazoles from Ynamides by Intramolecular Dehydro Diels−Alder Reactions
Martínez-Esperón, M. F., Rodrı́guez, D., Castedo, L., & Saá, C. (2005) · Organic Letters · doi:10.1021/ol050609a · Cited by 107
Iron-Catalyzed Amidation of Alkynyl Bromides: A Facile Route for the Preparation of Ynamides
Yao, B., Liang, Z., Niu, T., & Zhang, Y. (2009) · The Journal of Organic Chemistry · doi:10.1021/jo900595c · Cited by 106
Self-citationWitulski, B., Stengel, T., & Fernandez-Hernandez, J. M. (2000) · Chemical Communications · doi:10.1039/b005636g · Cited by 106
Witulski, B., Buschmann, N., & Bergsträßer, U. (2000) · Tetrahedron · doi:10.1016/s0040-4020(00)00773-0 · Cited by 106
A triazole-templated ring-closing metathesis for constructing novel fused and bridged triazoles
Zhang, X., Hsung, R. P., & Li, H. (2007) · Chemical Communications · doi:10.1039/b701040k · Cited by 105
Self-citationLindhardt, A. T., Mantel, M. L. H., & Skrydstrup, T. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200705558 · Cited by 97
Synthesis of α-Keto-Imides via Oxidation of Ynamides
Al-Rashid, Z. F., Johnson, W. L., Hsung, R. P., Wei, Y., Yao, P., Liu, R., & Zhao, K. (2008) · The Journal of Organic Chemistry · doi:10.1021/jo8015067 · Cited by 97
Self-citationSaito, N., Katayama, T., & Sato, Y. (2008) · Organic Letters · doi:10.1021/ol801534e · Cited by 97
Oppenheimer, J., Johnson, W. L., Tracey, M. R., Hsung, R. P., Yao, P., Liu, R., & Zhao, K. (2007) · Organic Letters · doi:10.1021/ol0707362 · Cited by 95
Self-citationA Sequential Metal-Catalyzed C−N Bond Formation in the Synthesis of 2-Amido-indoles
Yao, P., Zhang, Y., Hsung, R. P., & Zhao, K. (2008) · Organic Letters · doi:10.1021/ol801711p · Cited by 94
Self-citationApplication of Ynamides in the Synthesis of 2-Amidoindoles
Dooleweerdt, K., Ruhland, T., & Skrydstrup, T. (2008) · Organic Letters · doi:10.1021/ol802477d · Cited by 93
Zhang, Y., DeKorver, K. A., Lohse, A. G., Zhang, Y., Huang, J. Q., & Hsung, R. P. (2009) · Organic Letters · doi:10.1021/ol802844z · Cited by 92
Self-citationFirst total synthesis of antiostatin A1, a potent carbazole-based naturally occurring antioxidant
Alayrac, C., Schollmeyer, D., & Witulski, B. (2009) · Chemical Communications · doi:10.1039/b820291e · Cited by 92
Gourdet, B., Rudkin, M. E., Watts, C., & Lam, H. W. (2009) · The Journal of Organic Chemistry · doi:10.1021/jo901658v · Cited by 91
Gold-catalyzed cycloisomerizations of ene-ynamides
Couty, S., Meyer, C., & Cossy, J. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.10.108 · Cited by 85
Ruthenium-Catalyzed [2 + 2] Cycloadditions of Ynamides
Riddell, N., Villeneuve, K., & Tam, W. (2005) · Organic Letters · doi:10.1021/ol0512841 · Cited by 85
Copper Salt‐Catalyzed Azide‐[3 + 2] Cycloadditions of Ynamides and Bis‐Ynamides
Zhang, X., Li, H., You, L., Tang, Y. P., & Hsung, R. P. (2006) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200600404 · Cited by 85
Self-citationOppilliart, S., Mousseau, G., Zhang, L., Jia, G., Thuéry, P., Rousseau, B., & Cintrat, J. (2007) · Tetrahedron · doi:10.1016/j.tet.2007.06.008 · Cited by 84
Tanaka, R., Hirano, S., Urabe, H., & Sato, F. (2002) · Organic Letters · doi:10.1021/ol027209x · Cited by 83
Irregularities in the Effect of Potassium Phosphate in Ynamide Synthesis
Dooleweerdt, K., Birkedal, H., Ruhland, T., & Skrydstrup, T. (2008) · The Journal of Organic Chemistry · doi:10.1021/jo801935b · Cited by 81
Witulski, B., & Gößmann, M. (1999) · Chemical Communications · doi:10.1039/a905898b · Cited by 80
Garcia, P., Moulin, S., Miclo, Y., Lebœuf, D., Gandon, V., Aubert, C., & Malacrìa, M. (2009) · Chemistry - A European Journal · doi:10.1002/chem.200802301 · Cited by 79
Synthesis of Ketene N , N -Acetals by Copper-Catalyzed Double-Amidation of 1,1-Dibromo-1-alkenes
Coste, A., Couty, F., & Evano, G. (2009) · Organic Letters · doi:10.1021/ol901831s · Cited by 77
Hirano, S., Tanaka, R., Urabe, H., & Sato, F. (2004) · Organic Letters · doi:10.1021/ol036396b · Cited by 77
Frederick, M. O., Hsung, R. P., Lambeth, R. H., Mulder, J. A., & Tracey, M. R. (2003) · Organic Letters · doi:10.1021/ol030061c · Cited by 76
Self-citationKim, J. Y., Kim, S. H., & Chang, S. (2008) · Tetrahedron Letters · doi:10.1016/j.tetlet.2008.01.073 · Cited by 73
The Synthesis and Chemoselective Reactivity of 3-Aminocyclopentadienones
Rainier, J. D., & Imbriglio, J. E. (2000) · The Journal of Organic Chemistry · doi:10.1021/jo001044t · Cited by 73
Synthesis and Reactions of N-Ethynyl-heterocycles
KATRITZKY, A. R., Jiang, R., & Singh, S. K. (2004) · Heterocycles · doi:10.3987/rev-04-575 · Cited by 73
Marion, F., Courillon, C., & Malacrìa, M. (2003) · Organic Letters · doi:10.1021/ol036177q · Cited by 72
Highly Substituted 2-Amido-furans From Rh(II)-Catalyzed Cyclopropenations of Ynamides
Li, H., & Hsung, R. P. (2009) · Organic Letters · doi:10.1021/ol901860b · Cited by 70
Self-citationSynthesis of carbazoles by dehydro Diels–Alder reactions of ynamides
Martínez-Esperón, M. F., Rodrı́guez, D., Castedo, L., & Saá, C. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.02.029 · Cited by 68
Zhang, Y. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.079 · Cited by 68
Self-citationSynthesis and Chemoselective Reactivity of 3-Aminocyclopentadienones
Rainier, J. D., & Imbriglio, J. E. (1999) · Organic Letters · doi:10.1021/ol9912128 · Cited by 66
Laroche, C., Li, J., Freyer, M. W., & Kerwin, S. M. (2008) · The Journal of Organic Chemistry · doi:10.1021/jo801118q · Cited by 65
Zhang, Y. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.07.098 · Cited by 65
Self-citationTracey, M. R., Zhang, Y., Frederick, M. O., Mulder, J. A., & Hsung, R. P. (2004) · Organic Letters · doi:10.1021/ol0493251 · Cited by 63
Self-citationRuthenium-Catalyzed [2 + 2 + 2] Cocyclization of Diene-yne
Tanaka, D., Sato, Y., & Mori, M. (2007) · Journal of the American Chemical Society · doi:10.1021/ja071954t · Cited by 62
Bendikov, M., Duong, H. M., Bolanos, E., & Wudl, F. (2005) · Organic Letters · doi:10.1021/ol0477327 · Cited by 60
Radical cascade cyclizations and platinum(II)-catalyzed cycloisomerizations of ynamides
Marion, F., Coulomb, J., Servais, A., Courillon, C., Fensterbank, L., & Malacrìa, M. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.092 · Cited by 60
Hoffmann, R. W., & Brückner, D. B. (2001) · New Journal of Chemistry · doi:10.1039/b009259m · Cited by 57
Kohnen, A. L., Mak, X. Y., Lam, T. Y., Dunetz, J. R., & Danheiser, R. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.088 · Cited by 55
Zhang, X., Hsung, R. P., & You, L. (2006) · Organic & Biomolecular Chemistry · doi:10.1039/b606680a · Cited by 55
Self-citationPush-Pull Ynamines via Alkynyliodonium Chemistry
Murch, P., Williamson, B. L., & Stang, P. J. (1994) · Synthesis · doi:10.1055/s-1994-25675 · Cited by 55
Synthesis of cyclic dienamide using ruthenium-catalyzed ring-closing metathesis of ene–ynamide
Mori, M., Wakamatsu, H., Saito, N., Sato, Y., Sato, Y., Narita, R., Sato, Y., Sato, Y., & Fujita, R. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.083 · Cited by 53
Oppenheimer, J., Johnson, W. L., Figueroa, R., Hayashi, R., & Hsung, R. P. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.03.078 · Cited by 52
Self-citationReaction of Secondary Acetamides with N‐Dichloromethylene‐N,N‐dimethylammonium Chloride
Janoušek, Z., Collard, J., & Viehe, H. G. (1972) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197209171 · Cited by 50
Witulski, B., Lumtscher, J., & Bergsträßer, U. (2003) · Synlett · doi:10.1055/s-2003-38357 · Cited by 50
Martínez-Esperón, M. F., Rodrı́guez, D., Castedo, L., & Saá, C. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.082 · Cited by 49
A short synthesis of lennoxamine via ynamides
Couty, S., Meyer, C., & Cossy, J. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.11.093 · Cited by 49
Shen, L., & Hsung, R. P. (2003) · Tetrahedron Letters · doi:10.1016/j.tetlet.2003.10.064 · Cited by 48
Self-citationYasui, H., Yorimitsu, H., & Oshima, K. (2008) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.81.373 · Cited by 48
Ruthenium-catalyzed [2+2] cycloadditions of bicyclic alkenes and ynamides
Villeneuve, K., Riddell, N., & Tam, W. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.081 · Cited by 48
Stereoselective Synthesis of 1,2-Aminoalcohols by [2,3]-Wittig Rearrangements
Barbazanges, M., Meyer, C., & Cossy, J. (2007) · Organic Letters · doi:10.1021/ol0711725 · Cited by 48
Al-Rashid, Z. F., & Hsung, R. P. (2008) · Organic Letters · doi:10.1021/ol703083k · Cited by 47
Self-citationIJsselstijn, M., & Cintrat, J. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.090 · Cited by 47
New and Efficient Synthesis of Stannyl Enamines
Minière, S., & Cintrat, J. (2001) · Synthesis · doi:10.1055/s-2001-12779 · Cited by 46
Tracey, M. R., Oppenheimer, J., & Hsung, R. P. (2006) · The Journal of Organic Chemistry · doi:10.1021/jo061683p · Cited by 45
Self-citationNotes: An Unusual Reaction of Propargyl Bromide
Zaugg, H. E., Swett, L. R., & Stone, G. (1958) · The Journal of Organic Chemistry · doi:10.1021/jo01103a617 · Cited by 45
Kohnen, A. L., Dunetz, J. R., & Danheiser, R. (2007) · Organic Syntheses · doi:10.15227/orgsyn.084.0088 · Cited by 44
Shindo, N., Takemoto, Y., & Takasu, K. (2009) · Chemistry - A European Journal · doi:10.1002/chem.200901103 · Cited by 44
Synthesis of ynamides from formamides
Brückner, D. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.091 · Cited by 42
Kurtz, K. C. M., Frederick, M. O., Lambeth, R. H., Mulder, J. A., Tracey, M. R., & Hsung, R. P. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.087 · Cited by 42
Self-citation(2007) · Organic Syntheses · doi:10.15227/orgsyn.084.0359 · Cited by 41
Tanaka, K., & Takeishi, K. (2007) · Synthesis · doi:10.1055/s-2007-983799 · Cited by 40
Yasui, H., Yorimitsu, H., & Oshima, K. (2006) · Chemistry Letters · doi:10.1246/cl.2007.32 · Cited by 39
Gold(I)-catalyzed [4+2] cycloaddition of N-(hex-5-enynyl) tert-butyloxycarbamates
Buzas, A. K., Istrate, F. M., Goff, X. F. L., Odabachian, Y., & Gagosz, F. (2008) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2008.11.004 · Cited by 38
Hirano, S., Fukudome, Y., Tanaka, R., Sato, F., & Urabe, H. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.080 · Cited by 33
Hsung, R. P., Li, H., You, L., Zhang, X., Johnson, W. L., & Figueroa, R. (2007) · Heterocycles · doi:10.3987/com-07-s(w)34 · Cited by 32
Self-citationHighly regio- and stereocontrolled synthesis of β-substituted α-tributylstannyl enamides
Buissonneaud, D., & Cintrat, J. (2006) · Tetrahedron Letters · doi:10.1016/j.tetlet.2006.02.141 · Cited by 32
Synthesis and thermal cyclization of an enediyne-sulfonamide
Klein, M., & König, B. (2004) · Tetrahedron · doi:10.1016/j.tet.2003.11.078 · Cited by 31
Kanemura, S., Kondoh, A., Yasui, H., Yorimitsu, H., & Oshima, K. (2008) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.81.506 · Cited by 30
Thermal cyclization of 1,2-dialkynylimidazoles to imidazo[1,2-a]pyridines
Nadipuram, A. K., & Kerwin, S. M. (2006) · Tetrahedron · doi:10.1016/j.tet.2005.11.084 · Cited by 30
Structure and stability of enediynes containing heteroatoms—a quantum chemical investigation
Kraka, E., & Cremer, D. (2000) · Journal of Molecular Structure THEOCHEM · doi:10.1016/s0166-1280(00)00412-7 · Cited by 30
Barbazanges, M., Meyer, C., & Cossy, J. (2008) · Tetrahedron Letters · doi:10.1016/j.tetlet.2008.03.023 · Cited by 28
Yasui, H., Yorimitsu, H., & Oshima, K. (2007) · Chemistry Letters · doi:10.1246/cl.2008.40 · Cited by 26
Lithiation and functionalization of 1-alkynylimidazoles at the 2-position
Laroche, C., & Kerwin, S. M. (2009) · Tetrahedron Letters · doi:10.1016/j.tetlet.2009.06.133 · Cited by 25
Poloukhtine, A. A., & Popik, V. V. (2007) · Journal of the American Chemical Society · doi:10.1021/ja073614d · Cited by 24
Ruthenium-Catalyzed Alkenylative Cyclization via Insertion of Alkene into Ruthenacyclopentene
Mori, M., Tanaka, D., Saito, N., & Sato, Y. (2008) · Organometallics · doi:10.1021/om8008266 · Cited by 24
Clark, T., & Woerpel, K. A. (2005) · Organometallics · doi:10.1021/om050501z · Cited by 22
5H-Cyclopentapyrazines from 1,2-Dialkynylimidazoles
Kerwin, S. M., & Nadipuram, A. K. (2004) · Synlett · doi:10.1055/s-2004-825628 · Cited by 22
Research works printed but not linked: 88
- Bode J., 1892, Ann., 267, 268
- Klages F., 1941, Ann., 547, 65
- Wolf V., 1960, Ann., 638, 33
- Viehe H. G., 1963, Angew. Chem., Int. Ed. Engl., 2, 477, 10.1002/anie.196304771 · doi:10.1002/anie.196304771
- Viehe H. G., 1967, Angew. Chem., Int. Ed. Engl., 6, 767, 10.1002/anie.196707671 · doi:10.1002/anie.196707671
- Viehe, H. G.Chemistry of Acetylenes;Marcel Dekker:New York, 1969; Chapter 12, pp861−912.
- Pitacco, G. and Valentin, E.Chemistry of Functional Groups; 1979; Chapter 15,pp623−714.
- Collard-Motte J., 1986, Top. Curr. Chem., 130, 89, 10.1007/3-540-15810-3_3 · doi:10.1007/3-540-15810-3_3
- Himbert, G.InMethoden Der Organischen Chemie (Houben-Weyl);Kropf, H., and Schaumann, E., Eds.Georg Thieme Verlag:Stuttgart, 1993; p3267.
- Mulder J. A., 2003, Synlett, 1379
- Genet J. P., 1980, Tetrahedron Lett., 1521, 10.1016/S0040-4039(00)92763-1 · doi:10.1016/s0040-4039(00)92763-1
- van Elburg P. A., 1987, Tetrahedron Lett., 6397, 10.1016/S0040-4039(01)91385-1 · doi:10.1016/s0040-4039(01)91385-1
- Fischer H., 1997, J. Organomet. Chem., 541, 321, 10.1016/S0022-328X(97)00075-2 · doi:10.1016/s0022-328x(97)00075-2
- Balsells J., 2000, J. Org. Chem., 65, 7291, 10.1021/jo000278+ · doi:10.1021/jo000278+
- Katritzky A. R., 2006, Tetrahedron, 63, 3794, 10.1016/j.tet.2005.11.085 · doi:10.1016/j.tet.2005.11.085
- Ishihara T., 2006, Tetrahedron, 63, 3783, 10.1016/j.tet.2005.11.086 · doi:10.1016/j.tet.2005.11.086
- Goffin E., 1977, J. Chem. Res., Synop., 105
- Hsung R. P., 2006, Tetrahedron, 62, 3781, 10.1016/j.tet.2006.01.076 · doi:10.1016/j.tet.2006.01.076
- Ficini J., 1979, J. Am. Chem. Soc., 101, 1318, 10.1021/ja00499a063 · doi:10.1021/ja00499a063
- Kitamura T., 1998, Tetrahedron Lett., 39, 3787, 10.1016/S0040-4039(98)00617-0 · doi:10.1016/s0040-4039(98)00617-0
- Kitamura T., 2000, Heterocycles, 52, 303, 10.3987/COM-99-S25 · doi:10.3987/com-99-s25
- Balsamo A., 1985, Tetrahedron Lett., 26, 4141, 10.1016/S0040-4039(00)89314-4 · doi:10.1016/s0040-4039(00)89314-4
- Petersen L. I., 1968, Tetrahedron Lett., 9, 5357, 10.1016/S0040-4039(00)75383-4 · doi:10.1016/s0040-4039(00)75383-4
- Galy G. P., 1979, Synthesis, 944, 10.1055/s-1979-28881 · doi:10.1055/s-1979-28881
- Mahamoud A., 1981, Synthesis, 917, 10.1055/s-1981-29651 · doi:10.1055/s-1981-29651
- Katritzky A. R., 1985, J. Org. Chem., 50, 852, 10.1021/jo00206a026 · doi:10.1021/jo00206a026
- Majumdar K. C., 1994, Synth. Commun., 24, 217, 10.1080/00397919408013821 · doi:10.1080/00397919408013821
- Janousek Z., 1972, Angew. Chem., Int. Ed., 11, 917, 10.1002/anie.197209171 · DOI
- Joshi R. V., 1994, J. Chem. Soc., Perkin Trans. 1, 1089, 10.1039/p19940001089 · doi:10.1039/p19940001089
- Brückner D., 2000, Synlett, 1402
- Rodríguez D., 2004, Synlett, 783
- Rodriguez D., 2007, Synlett, 1963
- Couty S., 2005, Synlett, 905
- Murch P., 1994, Synthesis, 1255, 10.1055/s-1994-25675 · DOI
- Zhdankin V. V., 1998, Tetrahedron, 54, 10927, 10.1016/S0040-4020(98)00410-4 · DOI · Paper page
- Feldman K. S., 1996, J. Org. Chem., 61, 5440, 10.1021/jo9605814 · DOI
- Witulski B., 2000, Synlett, 1793
- cWitulski, B., Schweikert, T., Schollmeyer, D., and Nemkovich, N. A.Chem. Commun.,2010,http://dx.doi.org/DOI: 10.1039/b919275a. · doi:10.1039/b919275a
- Denonne F., 2003, Helv. Chim. Acta, 86, 3096, 10.1002/hlca.200390252 · doi:10.1002/hlca.200390252
- Balsamo A., 1985, Tetrahedron Lett., 26, 4141, 10.1016/S0040-4039(00)89314-4 · doi:10.1016/s0040-4039(00)89314-4
- Shen W., 1999, J. Org. Chem., 64, 8873, 10.1021/jo991116k · doi:10.1021/jo991116k
- Ghose S., 1991, J. Chem. Soc., Perkin Trans. 1, 775, 10.1039/p19910000775 · doi:10.1039/p19910000775
- Schottelius M., 1998, Helv. Chim. Acta, 81, 2341, 10.1002/(SICI)1522-2675(19981216)81:12<2341::AID-HLCA2341>3.0.CO;2-U · doi:10.1002/(sici)1522-2675(19981216)81:12<2341::aid-hlca2341>3.0.co;2-u
- Fromont C., 1999, Tetrahedron, 55, 5405, 10.1016/S0040-4020(99)00219-7 · doi:10.1016/s0040-4020(99)00219-7
- Mézailles N., 2005, Org. Lett., 7, 4133, 10.1021/ol0515917 · doi:10.1021/ol0515917
- Minière S., 2001, J. Org. Chem., 66, 7385, 10.1021/jo015824t · doi:10.1021/jo015824t
- Timbart L., 2002, Chem.—Eur. J., 8, 1637, 10.1002/1521-3765(20020402)8:7<1637::AID-CHEM1637>3.0.CO;2-7 · doi:10.1002/1521-3765(20020402)8:7<1637::aid-chem1637>3.0.co;2-7
- Naud S., 2003, Synthesis, 1391
- Chechik-Lankin H., 2005, Synlett, 2098
- Koester D. C., 2009, Angew. Chem., Int. Ed., 48, 7971, 10.1002/anie.200903773 · doi:10.1002/anie.200903773
- Charette A. B., 2000, J. Am. Chem. Soc., 122, 4508, 10.1021/ja994371v · doi:10.1021/ja994371v
- Sato A., 2009, Synlett, 28
- Bergman R. G., 1973, J. Am. Chem. Soc., 6, 25
- Kraka E., 2000, J. Am. Chem. Soc., 122, 8245, 10.1021/ja001017k · doi:10.1021/ja001017k
- Couty S., 2007, Synlett, 2819
- Al-Rashid, Z. F., Hsung, R. P., Antoline, J. E., Ko, C., Wei, Y., and Yang, J.40th ACS National Organic Symposium, Durham, NC, June 3, 2007, Abstract No. A-11.
- Cockburn N., 2009, J. Org. Chem., 74, 5762, 10.1021/jo9010206 · doi:10.1021/jo9010206
- Riddell N., 2009, J. Org. Chem., 74, 5762, 10.1021/jo9010206 · doi:10.1021/jo9010206
- Kohnen A. L., 2006, Tetrahedron, 62, 3815, 10.1016/j.tet.2005.11.088 · DOI
- Hsung R. P., 1999, Org. Lett., 1, 1237, 10.1021/ol990211c · doi:10.1021/ol990211c
- You L., 2007, Synlett, 1656
- Zhang X., 2006, Adv. Synth. Catal., 348, 2437, 10.1002/adsc.200600404 · DOI
- Zhang X., 2008, Org. Lett., 10, 3477, 10.1021/ol801257j · doi:10.1021/ol801257j
- Witulski B., 2000, Synlett, 12, 1793
- Domínguez G., 2002, Helv. Chim. Acta, 85, 2856, 10.1002/1522-2675(200209)85:9<2856::AID-HLCA2856>3.0.CO;2-5 · doi:10.1002/1522-2675(200209)85:9<2856::aid-hlca2856>3.0.co;2-5
- Gupta A. K., 2005, Tetrahedron Lett., 46, 4171, 10.1016/j.tetlet.2005.04.071 · doi:10.1016/j.tetlet.2005.04.071
- Witulski B., 1999, Angew. Chem., Int. Ed., 38, 2426, 10.1002/(SICI)1521-3773(19990816)38:16<2426::AID-ANIE2426>3.0.CO;2-Y · DOI · Paper page
- Friedman R. K., 2009, J. Am. Chem. Soc., 131, 10775, 10.1021/ja903899c · doi:10.1021/ja903899c
- Marion F., 2006, Tetrahedron, 62, 3856, 10.1016/j.tet.2005.11.092 · DOI
- Soriano E., 2005, J. Org. Chem., 70, 9345, 10.1021/jo0514265 · doi:10.1021/jo0514265
- Buzas A., 2009, Tetrahedron, 65, 1889, 10.1016/j.tet.2008.11.108 · doi:10.1016/j.tet.2008.11.108
- Lin G.-Y., 2008, Org. Lett., 10, 5059, 10.1021/ol802047g · doi:10.1021/ol802047g
- Saucy G., 1958, Helv. Chim. Acta, 41, 160, 10.1002/hlca.660410120 · doi:10.1002/hlca.660410120
- Marbet R., 1960, Chimia, 14, 361, 10.2533/chimia.1960.362_2 · doi:10.2533/chimia.1960.362_2
- Jones E. R. H., 1960, Proc. Chem. Soc., 180
- Huang J., 2002, Org. Lett., 4, 2417, 10.1021/ol020097p · DOI
- Rosillo M., 2004, J. Org. Chem., 69, 2084, 10.1021/jo0356311 · doi:10.1021/jo0356311
- Saito S., 2000, J. Org. Chem., 65, 4338, 10.1021/jo000171m · doi:10.1021/jo000171m
- Rodriguez D., 2004, Synlett, 377
- Xu X., 2007, Org. Lett., 9, 1585, 10.1021/ol070485x · doi:10.1021/ol070485x
- Yoo E. J., 2006, Org. Lett., 8, 1347, 10.1021/ol060056j · doi:10.1021/ol060056j
- Cui S.-L., 2006, Org. Lett., 8, 4517, 10.1021/ol061685w · doi:10.1021/ol061685w
- Cui S.-L., 2007, Org. Lett., 9, 5023, 10.1021/ol702241e · doi:10.1021/ol702241e
- Cui S.-L., 2008, Org. Lett., 10, 1267, 10.1021/ol800160q · doi:10.1021/ol800160q
- Jin Y., 2007, Synlett, 901
- DeKorver, K. A., Hsung, R. P., Lohse, A. G., and Zhang, Y.Org. Lett.2010,12, 1840. · doi:10.1021/ol100446p
- Yamasaki R., 2010, J. Org. Chem., 75, 480, 10.1021/jo902251m · doi:10.1021/jo902251m
- Burley G. A., 2010, J. Org. Chem., 75, 980, 10.1021/jo902466f · doi:10.1021/jo902466f
Cited by
Ynamides in Ring Forming Transformations
Wang, X.-N., Yeom, H.-S., Fang, L.-C., He, S., Ma, Z.-X., Kedrowski, B. L., & Hsung, R. P. (2014) · Accounts of Chemical Research · doi:10.1021/ar400193g · Cited by 605
Self-citationSilver-catalysed reactions of alkynes: recent advances
Fang, G., & Bi, X. (2015) · Chemical Society Reviews · doi:10.1039/c5cs00027k · Cited by 572
Reversal of Regioselectivity in Ynamide Chemistry
Zhou, B., Tan, T.-D., Zhu, X.-Q., Shang, M., & Ye, L.-W. (2019) · ACS Catalysis · doi:10.1021/acscatal.9b01851 · Cited by 294
Ynamides as Racemization-Free Coupling Reagents for Amide and Peptide Synthesis
Hu, L., Xu, S., Zhao, Z., Yang, Y., Peng, Z., Yang, M., Wang, C., & Zhao, J. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b07230 · Cited by 267
Palladium-catalyzed hydroacyloxylation of ynamides
Smith, D. L., Goundry, W. R. F., & Lam, H. W. (2012) · Chem. Commun. · doi:10.1039/c1cc13595c · Cited by 95
Metadata
- Authors
- DeKorver, K. A., Li, H., Lohse, A. G., Hayashi, R., Lu, Z., Zhang, Y., & Hsung, R. P.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2010-04-29
- Volume
- 110
- Issue
- 9
- Pages
- 5064-5106
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2061154455
- Cited by
- 886
- References
- 132
- FWCI
- 1.92
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.