The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Semipinacol Rearrangement in Natural Product Synthesis
Open accessAbstract
ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTSemipinacol Rearrangement in Natural Product SynthesisZhen-Lei Song†‡, Chun-An Fan‡, and Yong-Qiang Tu*‡View Author Information† Key Laboratory of Drug-Targeting of Education Ministry and Department of Medicinal Chemistry, West China School of Pharmacy, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, P. R. China.‡ State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China.Tel.: +86-931-8912385. Fax: +86-931-8912582. E-mail: [email protected]Cite this: Chem. Rev. 2011, 111, 11, 7523–7556Publication Date (Web):August 18, 2011Publication History Received16 February 2011Published online18 August 2011Published inissue 9 November 2011https://pubs.acs.org/doi/10.1021/cr200055ghttps://doi.org/10.1021/cr200055greview-articleACS PublicationsCopyright © 2011 American Chemical SocietyRequest reuse permissionsArticle Views23411Altmetric-Citations429LEARN 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:Alcohols,Chemical synthesis,Ketones,Organic synthesis,Rearrangement 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
Cascade Reactions in Total Synthesis
Nicolaou, K. C., Edmonds, D. J., & Bulger, P. G. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200601872 · Cited by 2,101
Asymmetric Organocatalytic Domino Reactions
Enders, D., Grondal, C., & Hüttl, M. R. M. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200603129 · Cited by 1,624
Organocatalytic cascade reactions as a new tool in total synthesis
Grondal, C., Jeanty, M., & Enders, D. (2010) · Nature Chemistry · doi:10.1038/nchem.539 · Cited by 1,582
Mechanisms Of Epoxide Reactions
Parker, R. E., & ISAACS, N. S. (1959) · Chemical Reviews · doi:10.1021/cr50028a006 · Cited by 1,178
Tandem reactions, cascade sequences, and biomimetic strategies in total synthesis
Nicolaou, K. C., Montagnon, T., & Snyder, S. A. (2003) · Chemical Communications · doi:10.1039/b209440c · Cited by 614
Stereoselective formation of quaternary carbon centers and related functions
Denissova, I., & Barriault, L. (2003) · Tetrahedron · doi:10.1016/j.tet.2003.10.039 · Cited by 495
Steven, A., & Overman, L. E. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200700612 · Cited by 464
Lindquist, N., Fenical, W., Duyne, G. D. V., & Clardy, J. (1991) · Journal of the American Chemical Society · doi:10.1021/ja00006a060 · Cited by 343
Enzymology and Molecular Biology of Aflatoxin Biosynthesis
Minto, R. E., & Townsend, C. A. (1997) · Chemical Reviews · doi:10.1021/cr960032y · Cited by 260
Total Synthesis of Nominal Diazonamides-Part 2: On the True Structure and Origin of Natural Isolates
Li, J., Burgett, A. W. G., Esser, L., Amezcua, C. A., & Harran, P. G. (2001) · Angewandte Chemie International Edition · Cited by 189
Biosynthesis of Prenylated Alkaloids Derived from Tryptophan
Williams, R. M., Stocking, E. M., & Sanz-Cervera, J. F. (2000) · Topics in Current Chemistry · doi:10.1007/3-540-48146-x_3 · Cited by 168
Synthesis and Structure Revision of Nakiterpiosin
Gao, S., Wang, Q., & Chen, C. (2008) · Journal of the American Chemical Society · doi:10.1021/ja808110d · Cited by 152
Gerard, B., Sangji, S., O’Leary, D. J., & Porco, J. A. J. (2006) · Journal of the American Chemical Society · doi:10.1021/ja062621j · Cited by 149
Gerard, B., Jones, G., & Porco, J. A. J. (2004) · Journal of the American Chemical Society · doi:10.1021/ja044798o · Cited by 142
Enantioselective Synthesis of the Complex Rocaglate (−)‐Silvestrol
Gerard, B., Cencic, R., Pelletier, J., & Porco, J. A. J. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200702707 · Cited by 118
Jeon, S., & Walsh, P. J. (2003) · Journal of the American Chemical Society · doi:10.1021/ja036302t · Cited by 103
Scalable Total Synthesis and Biological Evaluation of Haouamine A and Its Atropisomer
Burns, N. Z., Krylova, I. N., Hannoush, R. N., & Baran, P. S. (2009) · Journal of the American Chemical Society · doi:10.1021/ja903745s · Cited by 102
Chemical and Biological Studies of Nakiterpiosin and Nakiterpiosinone
Gao, S., Wang, Q., Huang, L. J.-S., Lum, L., & Chen, C. (2009) · Journal of the American Chemical Society · doi:10.1021/ja908626k · Cited by 84
Roche, S. P., Cencic, R., Pelletier, J., & Porco, J. A. J. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201003212 · Cited by 76
Tandem methodology for heterocyclic synthesis
Padwa, A. (2004) · Pure and Applied Chemistry · doi:10.1351/pac200476111933 · Cited by 73
Alcaide, B., Almendros, P., Luna, A., & Torres, M. R. (2010) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200900864 · Cited by 45
Iguchi, K., Shimada, Y., & Yamada, Y. (1992) · The Journal of Organic Chemistry · doi:10.1021/jo00028a023 · Cited by 37
Srikrishna, A., & Ramasastry, S. S. V. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.08.124 · Cited by 35
Yamano, Y., & Ito, M. (2007) · Organic & Biomolecular Chemistry · doi:10.1039/b710386g · Cited by 23
Tode, C., Yamano, Y., & Ito, M. (2002) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/b201228f · Cited by 18
Yamano, Y., Ito, M., & Wada, A. (2008) · Organic & Biomolecular Chemistry · doi:10.1039/b807482h · Cited by 16
Simpson, T. J., de Jesus, A. E., Steyn, P. S., et al. (1982) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39820000631 · Cited by 11
Yamano, Y., & Ito, M. (2001) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.49.1662 · Cited by 10
Yamano, Y., & Ito, M. (2004) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.52.780 · Cited by 9
Cited by
Dual Visible Light Photoredox and Gold-Catalyzed Arylative Ring Expansion
Shu, X.-Z., Zhang, M., He, Y., Frei, H., & Toste, F. D. (2014) · Journal of the American Chemical Society · doi:10.1021/ja500716j · Cited by 435
All-carbon quaternary centers in natural products and medicinal chemistry: recent advances
Ling, T., & Rivas, F. (2016) · Tetrahedron · doi:10.1016/j.tet.2016.09.002 · Cited by 312
Ecdysteroids: Isolation, Chemical Transformations, and Biological Activity
Savchenko, R. G., Veskina, N. A., Odinokov, V. N., Benkovskaya, G. V., & Parfenova, L. V. (2022) · Phytochemistry Reviews · doi:10.1007/s11101-021-09792-y · Cited by 39
In vitro adjuvant antitumor activity of various classes of semi-synthetic poststerone derivatives
Savchenko, R. G., Nové, M., Spengler, G., Hunyadi, A., & Parfenova, L. V. (2021) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2020.104485 · Cited by 8
Metadata
- Authors
- Song, Z.-L., Fan, C.-A., & Tu, Y.-Q.
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2011-08-18
- Volume
- 111
- Issue
- 11
- Pages
- 7523-7556
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W2318715057
- Cited by
- 544
- References
- 29
- FWCI
- 0.55
- 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.
