On the mechanism of the deoxygenation of secondary alcohols by the reduction of their methyl xanthates by tin hydrides

A new method for the deoxygenation of secondary alcohols

Barton, D. H. R., & McCombie, S. W. (1975) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19750001574 · Cited by 1,666

Modern methods for the radical deoxygenation of alcohols

Hartwig, W. (1983) · Tetrahedron · doi:10.1016/s0040-4020(01)91972-6 · Cited by 324

Steroids and sex hormones. Part 262. The radical induced stannane reduction of selenoesters and selenocarbonates: A new method for the degradation of carboxylic acids to nor‐alkanes and for desoxygenation of alcohols to alkanes

Pfenninger, J., Heuberger, C., & Graf, W. (1980) · Helvetica Chimica Acta · doi:10.1002/hlca.19800630823 · Cited by 113

Radical-Induced Deoxygenation of Primary Alcohols

Barton, D. H. R., Motherwell, W. B., & Stange, A. F. (1981) · Synthesis · doi:10.1055/s-1981-29587 · Cited by 110

Diaryl telluroxides as new mild oxidising reagents

Ley, S. V., Meerholz, C. A., & Barton, D. H. R. (1981) · Tetrahedron · doi:10.1016/0040-4020(81)85057-0 · Cited by 98

New and selective reactions and reagents in carbohydrate chemistry

Barton, D. H. R., & Motherwell, W. B. (1981) · Pure and Applied Chemistry · doi:10.1351/pac198153010015 · Cited by 88

Kinetic applications of electron paramagnetic resonance spectroscopy. 25. Radicals formed by spin trapping with di-tert-butyl thioketone

Scaiano, J. C., & Ingold, K. U. (1976) · Journal of the American Chemical Society · doi:10.1021/ja00432a006 · Cited by 81

On the mechanism of reduction of dithiocarbonates (xanthates) with tributylstannane

Barton, D. H. R., Crich, D., Löbberding, A., & Zard, S. Z. (1985) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39850000646 · Cited by 42

E.s.r. identification of alkoxythiocarbonyl radicals as possible intermediates in barton deoxygenation of alcohols

Barker, P. J., & Backwith, A. L. J. (1984) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39840000683 · Cited by 33

Preparation of some organotin compounds containing methylthio, phenylthio, and pentafluoro-phenylthio groups

Peach, M. E. (1968) · Canadian Journal of Chemistry · doi:10.1139/v68-033 · Cited by 28

Experimental Requirements for an Efficient Control of Free‐Radical Polymerizations via the Reversible Addition‐Fragmentation Chain Transfer (RAFT) Process

Favier, A., & Charreyre, M. (2006) · Macromolecular Rapid Communications · doi:10.1002/marc.200500839 · Cited by 462

On the Trail of Xanthates: Some New Chemistry from an Old Functional Group

Zard, S. Z. (1997) · Angewandte Chemie International Edition in English · doi:10.1002/anie.199706721 · Cited by 444

N-Heterocyclic Carbene Boryl Radicals: A New Class of Boron-Centered Radical

Ueng, S., Solovyev, A. Y., Yuan, X., Geib, S. J., Fensterbank, L., Lacôte, E., Malacrìa, M., Newcomb, M., Walton, J. C., & Curran, D. P. (2009) · Journal of the American Chemical Society · doi:10.1021/ja904103x · Cited by 323

Chemistry of β-(Acyloxy)alkyl and β-(Phosphatoxy)alkyl Radicals and Related Species: Radical and Radical Ionic Migrations and Fragmentations of Carbon−Oxygen Bonds

BECKWITH, A. L. J., Crich, D., Duggan, P. J., & Yao, Q. (1997) · Chemical Reviews · doi:10.1021/cr950207o · Cited by 138

Rapid Defunctionalization of Carbonyl Group to Methylene with Polymethylhydrosiloxane−B(C6F5)3

Chandrasekhar, S., Reddy, C. R., & Babu, B. N. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo0204045 · Cited by 127

O -Benzyl Xanthate Esters under Ni/Photoredox Dual Catalysis: Selective Radical Generation and Csp3–Csp2 Cross-Coupling

Vara, B., Patel, N. R., & Molander, G. A. (2017) · ACS Catalysis · doi:10.1021/acscatal.7b00772 · Cited by 124

Noncovalent Synthesis Using Hydrogen Bonding

Prins, L. J., Reinhoudt, D. N., & Timmerman, P. (2001) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20010702)40:13 · Cited by 1,219

The invention of radical reactions

Barton, D. H. R., Bridon, D. P., Fernandaz-Picot, I., & Zard, S. Z. (1987) · Tetrahedron · doi:10.1016/s0040-4020(01)86878-2 · Cited by 112

Polymerization of Ethylene through Reversible Addition–Fragmentation Chain Transfer (RAFT)

Dommanget, C., D’Agosto, F., & Monteil, V. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201403491 · Cited by 110

Radical chain reduction of alkyl halides, dialkyl sulphides and O-alkyl S-methyl dithiocarbonates to alkanes by trialkylsilanes

Cole, S. J., Kirwan, J. N., Roberts, B. P., & Willis, C. R. (1991) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19910000103 · Cited by 109

Facile reduction of dithiocarbonates with n-Bu3SnH-Et3B. Easy access to hydrocarbons from secondary alcohols

Nozaki, K., Oshima, K., & Utimoto, K. (1988) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)82283-2 · Cited by 92

A practical method for the reductive cleavage of the sulfide bond in xanthates

Liard, A., Quiclet‐Sire, B., & Zard, S. Z. (1996) · Tetrahedron Letters · doi:10.1016/0040-4039(96)01253-1 · Cited by 88

Chiral bipyrindine and biquinoline ligands: Their asymmetric synthesis and application to the synthesis of trans-whisky lactone

Ito, K., Yoshitake, M., & Katsuki, T. (1996) · Tetrahedron · doi:10.1016/s0040-4020(96)00058-0 · Cited by 88

Alkyl/Glycosyl Sulfoxides as Radical Precursors and Their Use in the Synthesis of Pyridine Derivatives**

Xie, D., Wang, Y., Zhang, X., Fu, Z., & Niu, D. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202204922 · Cited by 82

Chemistry of Porphyrin-Appended Cellulose Strands with a Helical Structure: Spectroscopy, Electrochemistry, and in situ Circular Dichroism Spectroelectrochemistry

Redl, F. X., Lutz, M., & Daub, J. (2001) · Chemistry - A European Journal · doi:10.1002/1521-3765(20011217)7:24 · Cited by 75

On the mechanism of deoxygenation of secondary alcohols by tin hydride reduction of methyl xanthates and other thiocarbonyl derivatives

Barton, D. H. R., Doo, O. J., & Jászberényi, J. C. (1990) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)94480-0 · Cited by 74

Deoxygenative Functionalization of Hydroxy Groups via Xanthates with Tetraphenyldisilane

Togo, H., Matsubayashi, S., Yamazaki, O., & Yokoyama, M. (2000) · The Journal of Organic Chemistry · doi:10.1021/jo991715r · Cited by 72

Regioselective Enolization and Alkylation of 4-Oxo-N-(9-phenylfluoren-9-yl)proline: Synthesis of Enantiopure Proline−Valine and Hydroxyproline−Valine Chimeras

Sharma, R. L., & Lubell, W. D. (1996) · The Journal of Organic Chemistry · doi:10.1021/jo9514984 · Cited by 71

Thiocarbonyl chemistry in polymer science

Bingham, N. M., Abousalman-Rezvani, Z., Collins, K., & Roth, P. J. (2022) · Polymer Chemistry · doi:10.1039/d2py00050d · Cited by 66

The Barton‐McCombie Reaction

McCombie, S. W., Motherwell, W. B., & Tozer, M. J. (2012) · Organic reactions · doi:10.1002/0471264180.or077.02 · Cited by 64

Auf der Spur von Xanthaten ‐ neue Chemie einer alten funktionellen Gruppe

Zard, S. Z. (1997) · Angewandte Chemie · doi:10.1002/ange.19971090706 · Cited by 63

The invention of radical reactions

Barton, D. H. R., Lacher, B., Misterkiewicz, B., & Zard, S. Z. (1988) · Tetrahedron · doi:10.1016/s0040-4020(01)85895-6 · Cited by 59

Progress of the Barton-McComble Methodology: From tin hydrides to Silanes

Chatgilialoglu, C., & Ferreri, C. (1993) · Research on Chemical Intermediates · doi:10.1163/156856793x00361 · Cited by 59

Acylcobalt salophen reagents. Precursors to acyl radical intermediates for use in carbon-to-carbon bond-forming reactions to alkenes

Coveney, D. J., Patel, V. F., Pattenden, G., & Thompson, D. M. (1990) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19900002721 · Cited by 59

Macromolecular Design by Interchange of Xanthates: Background, Design, Scope and Applications

Taton, D., Destarac, M., & Zard, S. Z. (2008) · doi:10.1002/9783527622757.ch10 · Cited by 58

Iridium-Catalyzed Highly Efficient and Site-Selective Deoxygenation of Alcohols

Yang, S., Tang, W., Yang, Z., & Xu, J. (2018) · ACS Catalysis · doi:10.1021/acscatal.8b02495 · Cited by 56

Deoxygenation of alcohols by the reactions of their xanthate esters with triethylsilane: An alternative to tributyltin hydride in the Barton-McCombie reaction

Kirwan, J. N., Roberts, B. P., & Willis, C. R. (1990) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)97814-6 · Cited by 56

A practical access to acyl radicals from acyl hydrazides

Bath, S., Laso, N. M., López-Ruíz, H., Quiclet‐Sire, B., & Zard, S. Z. (2002) · Chemical Communications · doi:10.1039/b210764c · Cited by 53

Safe, facile radical-based reduction and hydrosilylation reactions in a microreactor using tris(trimethylsilyl)silane

Odedra, A., Geyer, K., Tomas, G., Gilmour, R., & Seeberger, P. H. (2008) · Chemical Communications · doi:10.1039/b803715a · Cited by 53

Discovery of the RAFT/MADIX Process: Mechanistic Insights and Polymer Chemistry Implications

Zard, S. Z. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c01441 · Cited by 52

Direct Radical Copolymerizations of Thioamides To Generate Vinyl Polymers with Degradable Thioether Bonds in the Backbones

Watanabe, H., & Kamigaito, M. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c01796 · Cited by 51

Radical O→C Transposition: A Metal-Free Process for Conversion of Phenols into Benzoates and Benzamides

Baroudi, A., Alicea, J., Flack, P., Kirincich, J., & Alabugin, I. V. (2011) · The Journal of Organic Chemistry · doi:10.1021/jo102467j · Cited by 51

Reflections on the mechanism of the Barton-McCombie Deoxygenation and on its consequences†

McCombie, S. W., Quiclet-Sire, B., & Zard, S. Z. (2018) · Tetrahedron · doi:10.1016/j.tet.2018.03.042 · Cited by 48

Nichtkovalente Synthese mit Wasserstoffbrücken

Prins, L. J., Reinhoudt, D. N., & Timmerman, P. (2001) · Angewandte Chemie · doi:10.1002/1521-3757(20010702)113:13 · Cited by 238

Total Synthesis of (+)‐Machaeriol D with a Key Regio‐ and Stereoselective SN2′ Reaction

Wang, Q., Huang, Q., Chen, B., Lu, J., Wang, H., She, X., & Pan, X. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200600006 · Cited by 46

Aromatic Xanthates and Dithiocarbamates for the Polymerization of Ethylene through Reversible Addition–Fragmentation Chain Transfer (RAFT)

Wolpers, A., Bergerbit, C., Ebeling, B., D’Agosto, F., & Monteil, V. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201905629 · Cited by 44

The invention of radical reactions. Part XXXI. Diphenylsilane: a reagent for deoxygenation of alcohols via their thiocarbonyl derivatives, deamination via isonitriles, and dehalogenation of bromo- and iodo- compounds by radical chain chemistry

Barton, D. H. R., Jang, D. O., & Jászberényi, J. C. (1993) · Tetrahedron · doi:10.1016/s0040-4020(01)87198-2 · Cited by 44

A novel radical chain reaction of xanthic anhydrides. Further observations on the intermediacy of alkoxy-thiocarbonyl radicals in the Barton-McCombie reaction

Forbes, J. E., & Zard, S. Z. (1989) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)99362-6 · Cited by 41

Xanthates and Related Derivatives as Radical Precursors

Zard, S. Z. (2001) · doi:10.1002/9783527618293.ch6 · Cited by 41

Sulfamate Esters Guide C(3)-Selective Xanthylation of Alkanes

Ayer, S. K., & Roizen, J. L. (2019) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.9b00105 · Cited by 40

Enantiospecific Total Synthesis of (−)-4-Thiocyanatoneopupukeanane

Srikrishna, A., & Gharpure, S. J. (2001) · The Journal of Organic Chemistry · doi:10.1021/jo0102765 · Cited by 39

Total Synthesis of (15R)- and (15S)-F2t-Isoprostanes by a Biomimetic Process Using the Cyclization of Acyclic Dihydroxylated Octa-5,7-dienyl Radicals

Durand, T., Guy, A., Vidal, J., & Rossi, J. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo0109624 · Cited by 39

Synthesis of Deoxyglycosides by Desulfurization under UV Light

Ge, J., Li, Y., Tian, J. J., Liao, R., & Dong, H. (2017) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.7b00896 · Cited by 37

Enantiospecific total synthesis of phytoalexins, (+)-solanascone, (+)-dehydrosolanascone, and (+)-anhydro-β-rotunol

Srikrishna, A., & Ramasastry, S. S. V. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.08.124 · Cited by 35

Insertion of Degradable Thioester Linkages into Styrene and Methacrylate Polymers: Insights into the Reactivity of Thionolactones

Rix, M. F. I., Collins, K., Higgs, S. J., Dodd, E. M., Coles, S. J., Bingham, N. M., & Roth, P. J. (2023) · Macromolecules · doi:10.1021/acs.macromol.3c01811 · Cited by 46

A New Reaction Manifold for the Barton Radical Intermediates: Synthesis of N-Heterocyclic Furanosides and Pyranosides via the Formation of the C1−C2 Bond

Rhee, J. U., Bliss, B. I., & RajanBabu, T. V. (2003) · Journal of the American Chemical Society · doi:10.1021/ja028617z · Cited by 32

Total synthesis of 12-epi-PGF2α

Hwang, S., Adiyaman, M., Khanapure, S. P., & Rokach, J. (1996) · Tetrahedron Letters · doi:10.1016/0040-4039(95)02390-9 · Cited by 32

Facile Reduction of Dithiocarbonates Derived from Secondary Alcohols with n-Bu3SnH–Et3B and Synthesis of 2-Furanthiones and 2-Furanones by Intramolecular Addition of Alkoxythiocarbonyl Free Radicals to Acetylenic Linkages

Nozaki, K., Oshima, K., & Utimoto, K. (1990) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.63.2578 · Cited by 31

Metal‐Free Transformation of Phenols into Substituted Benzamides: A Highly Selective Radical 1,2‐O→C Transposition in O‐Aryl‐N‐phenylthiocarbamates

Baroudi, A., Flack, P., & Alabugin, I. V. (2010) · Chemistry - A European Journal · doi:10.1002/chem.201002303 · Cited by 30

Synthesis of 5,6,11-Trideoxytetrodotoxin

Adachi, M., Sakakibara, R., Satake, Y., Isobe, M., & Nishikawa, T. (2014) · Chemistry Letters · doi:10.1246/cl.140684 · Cited by 29

Bioinspired Synthesis of (−)‐PF‐1018

Quintela‐Varela, H., Jamieson, C. S., Shao, Q., Houk, K. N., & Trauner, D. H. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201912452 · Cited by 29

Radical 1,2‐O→C Transposition for Conversion of Phenols into Benzoates by O‐Neophyl Rearrangement/Fragmentation Cascade

Baroudi, A., Alicea, J., & Alabugin, I. V. (2010) · Chemistry - A European Journal · doi:10.1002/chem.201001056 · Cited by 27

Functionalized cyclopentanes via radical cyclizations using thiocarbonate derivatives as initiators and terminators

Ziegler, F. E., & Zheng, Z.-L. (1987) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)96840-0 · Cited by 27

A Convenient, High Yielding Cleavage of the Thiocarbonyl Group in Xanthates

Quiclet‐Sire, B., & Zard, S. Z. (2010) · Bulletin of the Korean Chemical Society · doi:10.5012/bkcs.2010.31.03.543 · Cited by 26

A synthesis of the abietane diterpenoid quinone (±)-royleanone via maleoylcobalt technology.

Liebeskind, L. S., Chidambaram, R., Nimkar, S., & Liotta, D. C. (1990) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)97454-9 · Cited by 26

Polymerization of Ethylene through Reversible Addition–Fragmentation Chain Transfer (RAFT)

Dommanget, C., D’Agosto, F., & Monteil, V. (2014) · Angewandte Chemie · doi:10.1002/ange.201403491 · Cited by 25

Degradable Diblock Copolymer Vesicles via Radical Ring-Opening Polymerization-Induced Self-Assembly in Aqueous Media

Georgiou, P. G., Neal, T. J., Newell, M. A., Hepburn, K. S., Tyler, J. J. S., Farmer, M. A. H., Chohan, P., Roth, P. J., Nicolas, J., & Armes, S. P. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c03744 · Cited by 25

A general route to 5,6-seco-hexahydrodibenzopyrans and analogues: first total synthesis of (+)-Machaeridiol B and (+)-Machaeriol B

Huang, Q., Wang, Q., Zheng, J., Zhang, J., Pan, X., & She, X. (2006) · Tetrahedron · doi:10.1016/j.tet.2006.10.067 · Cited by 24

Treasures from the Free Radical Renaissance Period – Miscellaneous hexenyl radical kinetic data

BECKWITH, A. L. J., & Schiesser, C. H. (2010) · Organic & Biomolecular Chemistry · doi:10.1039/c0ob00708k · Cited by 22

Xanthic anhydrides: A novel and convenient source of alkoxythiocarbonyl and alkyl radicals.

Forbes, J. E., & Zard, S. Z. (1993) · Tetrahedron · doi:10.1016/s0040-4020(01)88043-1 · Cited by 22

SYNTHESES OF AVENACIOLIDE AND RELATEDbisLACTONES. A REVIEW

Martı́n, V. S., Rodríguez, C. M., & Martı́n, T. (1998) · Organic Preparations and Procedures International · doi:10.1080/00304949809355291 · Cited by 22

Ruthenium‐Catalyzed O‐ to S‐Alkyl Migration: A Pseudoreversible Barton–McCombie Pathway

Mahy, W., Plucinski, P. K., Jover, J., & Frost, C. G. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201505280 · Cited by 21

Ring closure of the 6-methylenecyclodecyl radical

BECKWITH, A. L. J., Bowry, V. W., & Schiesser, C. H. (1991) · Tetrahedron · doi:10.1016/0040-4020(91)80014-s · Cited by 21

Ethers as hydrogen sources in BF 3 ·OEt 2 promoted reduction of diphenylmethyl alcohols, ethers and esters to hydrocarbons

Li, J., Liu, Q., Shen, H., Huang, R., Zhang, X., Xiong, Y., & Chen, C. (2015) · RSC Advances · doi:10.1039/c5ra14775a · Cited by 20

Synthesis of (+)-makassaric acid, a protein kinase MK2 inhibitor

Basabe, P., Martín, M., Bodero, O., Blanco, A., Marcos, I. S., David Diez, A., & Urones, J. G. (2010) · Tetrahedron · doi:10.1016/j.tet.2010.06.023 · Cited by 20

Enantiospecific synthesis of (−)-2-hydroxy-exo-brevicomin

Prasad, K. R., & Anbarasan, P. (2006) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2006.02.023 · Cited by 19

Red-Light-Mediated Barton–McCombie Reaction

Ogura, A., Ichii, N., Shibata, K., & Takao, K. (2020) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.20200087 · Cited by 17

Universal Group 14 Free Radical Photoinitiators for Vinylidene Fluoride, Styrene, Methyl Methacrylate, Vinyl Acetate, and Butadiene

Kim, J.-S., Dutta, A., Vasu, V., Adebolu, O. I., & Asandei, A. D. (2019) · Macromolecules · doi:10.1021/acs.macromol.9b01802 · Cited by 17

Oxygen–carbon β-bond effects in radical reactions

Jenkins, I. D. (1994) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39940001227 · Cited by 17

High yield reduction of 2-O-trifluoromethanesulphonate esters of α-hydroxylactones to the corresponding 2-deoxylactones by lithium iodide trihydrate

Elliott, R. P., Fleet, G. W. J., Young, S. G., Ramsden, N. G., & Smith, C. (1990) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)97471-9 · Cited by 17

Aromatic Xanthates and Dithiocarbamates for the Polymerization of Ethylene through Reversible Addition–Fragmentation Chain Transfer (RAFT)

Wolpers, A., Bergerbit, C., Ebeling, B., D’Agosto, F., & Monteil, V. (2019) · Angewandte Chemie · doi:10.1002/ange.201905629 · Cited by 16

One-step selective deoxygenation of alcohols from acyloins

Uranga, J. G., Chiosso, A. F., & Santiago, A. N. (2013) · RSC Advances · doi:10.1039/c3ra40343b · Cited by 16

On the use of S-(4-alkenyl)-dithiocarbonates as mechanistic probes in the barton-McCombie radical deoxygenation reaction

Crich, D. (1988) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)82197-8 · Cited by 16

Novel skeletal rearrangement of hydroindan derivatives into hydroazulenones via an alkoxy radical

Goto, M., Miyoshi, I., Ishii, Y., Ogasawara, Y., Kakimoto, Y., Nagumo, S., Nishida, A., Kawahara, N., & Nishida, M. (2002) · Tetrahedron · doi:10.1016/s0040-4020(02)00102-3 · Cited by 15

The invention of radical reactions. Part XXXV. A novel radical fission reaction of N-sulfonylthioxocarbamates

Barton, D. H. R., Fontana, G. A., & Yang, Y. Q. (1996) · Tetrahedron · doi:10.1016/0040-4020(95)01019-x · Cited by 15

Total synthesis of (±)-β-chamigrene and (±)-laurencenone C via Ireland ester Claisen rearrangement and an intramolecular type II carbonyl ene reaction sequence

Srikrishna, A., & Babu, R. R. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.08.095 · Cited by 14

Stereocontrolled Total Synthesis of Polygalolide A

Yamada, H., Adachi, M., Isobe, M., & Nishikawa, T. (2013) · Chemistry - An Asian Journal · doi:10.1002/asia.201300362 · Cited by 14

Regioselective sulfamoylation at low temperature enables concise syntheses of putative small molecule inhibitors of sulfatases

Miller, D. C., Carbain, B., Beale, G., Alhasan, S. F., Reeves, H. L., Baisch, U., Newell, D. R., Golding, B. T., & Griffin, R. J. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob00211g · Cited by 14

Synthesis of 2′,3′-Dideoxyribavirin

Sanghvi, Y. S., Hanna, N. B., Larson, S. B., Robins, R. K., & Revankar, G. R. (1987) · Nucleosides and Nucleotides · doi:10.1080/15257778708073422 · Cited by 13

The Radical Chemistry of Thiocarbonylthio Compounds: An Overview

Zard, S. Z. (2008) · doi:10.1002/9783527622757.ch5 · Cited by 13

Xanthates and Related Derivatives as Radical Precursors

Zard, S. Z. (2012) · Wiley eBooks · doi:10.1002/9781119953678.rad028 · Cited by 13

Insertion of Degradable Thioester Linkages into Styrene and Methacrylate PolymersPreprint

Rix, M. F. I., Higgs, S. J., Dodd, E. M., Coles, S. J., Bingham, N. M., & Roth, P. J. (2022) · ChemRxiv · doi:10.26434/chemrxiv-2022-cdt52 · Cited by 13

Mechanistic Perspectives on Stereocontrol in Lewis Acid-Mediated Radical Polymerization

Noble, B. B., & Coote, M. L. (2015) · Advances in physical organic chemistry · doi:10.1016/bs.apoc.2015.07.002 · Cited by 12

Iridium-catalyzed highly stereoselective deoxygenation of tertiary cycloalkanols: stereoelectronic insights and synthetic applications

Wang, T., Yang, C., Chen, N., Xu, J., & Yang, Z. (2021) · Organic & Biomolecular Chemistry · doi:10.1039/d1ob01690c · Cited by 12

Reductions of steroidal halohydrins and their esters by tri-n.butyltin hydride; some stereospecific 1.2-migrations of acetoxy- or benzoxy-groups

Julia, S. A., & Lorne, R. (1986) · Tetrahedron · doi:10.1016/s0040-4020(01)88052-2 · Cited by 11

Unusual generation of methoxy groups in Barton deoxygenations of alcohols

Bensasson, C. S., Cornforth, S. J., Du, M.-H., & Hanson, J. R. (1997) · Chemical Communications · doi:10.1039/a703156d · Cited by 11

Total Synthesis of Polygalolide A

Adachi, M., Yamada, H., Isobe, M., & Nishikawa, T. (2011) · Organic Letters · doi:10.1021/ol2028256 · Cited by 11

Skeletal Rearrangement via Alkoxy Radical: Conversion of Epoxydecalin Thiocarbonylimidazolides to Bicyclo[6.3.0]undecanones and Bicyclo[5.3.1]undecanones

Kakimoto, Y., Ogasawara, Y., Nishida, A., Kawahara, N., Nishida, M., & Takayanagi, H. (2000) · Tetrahedron · doi:10.1016/s0040-4020(00)00635-9 · Cited by 11

Redox-Active Thiocarbonyl Auxiliaries in Ni-Catalyzed Cross-Couplings of Aliphatic Alcohols

Monteith, J. J., & Rousseaux, S. A. L. (2023) · Accounts of Chemical Research · doi:10.1021/acs.accounts.3c00541 · Cited by 10

β-Oxygen Effect in the Barton–McCombie Deoxygenation Reaction: Further Experimental and Theoretical Findings

Sánchez-Eleuterio, A., Sandoval‐Lira, J., García-Sánchez, J., Monterrosas-Pérez, L., Hernández‐Pérez, J. M., Quintero, L., & Sartillo‐Piscil, F. (2013) · The Journal of Organic Chemistry · doi:10.1021/jo4012943 · Cited by 9

Lichtinduzierte Strukturänderungen während der Primärprozesse der Photosynthese: direkte Verfolgung einer Enzymreaktion

Huber, M. (1998) · Angewandte Chemie · doi:10.1002/(sici)1521-3757(19980420)110:8 · Cited by 2

Synthesis of 3′‐S‐Phosphonomethyl‐Modified Nucleoside Phosphonates with a 3′‐Deoxy‐3′‐thio‐α‐ L ‐threosyl Sugar Moiety

Huang, Q., & Herdewijn, P. A. (2011) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201100177 · Cited by 9

Synthesis of samanine

Cristofoli, W. A., & Benn, M. H. (1991) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19910001825 · Cited by 9

Stereochemical control in radical cyclization routes to N-glycosides: role of protecting groups and of the configuration (E versus Z) of the acceptors

Rhee, J. U., Bliss, B. I., & RajanBabu, T. V. (2003) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2003.07.013 · Cited by 8

Total Synthesis of (+)‐Machaeriol D with a Key Regio‐ and Stereoselective SN2′ Reaction

Wang, Q., Huang, Q., Chen, B., Lu, J., Wang, H. Z., She, X., & Pan, X. (2006) · Angewandte Chemie · doi:10.1002/ange.200600006 · Cited by 8

Radical-induced cyclization of the S-methyl dithiocarbonate of 1,2-O-isopropylidene-α-xylose

Herdewijn, P. A., Aerschot, A. A. V., Jie, L., Esmans, E. L., Feneau-Dupont, J., & Declercq, J. (1991) · Journal of the Chemical Society Perkin Transactions 1 · doi:10.1039/p19910001729 · Cited by 8

The Invention of Radical Chain Reactions of Value in Organic Synthesis

Minisci, F. (1990) · Springer eBooks · doi:10.1007/978-1-4684-5874-9_26 · Cited by 8

Bioinspired Synthesis of (−)‐PF‐1018

Quintela‐Varela, H., Jamieson, C. S., Shao, Q., Houk, K. N., & Trauner, D. H. (2019) · Angewandte Chemie · doi:10.1002/ange.201912452 · Cited by 7

Electron spin resonance study of free radicals generated from retinyl- and ionyl-derivatives

Mordi, R. C., & Walton, J. C. (1990) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(90)90062-v · Cited by 7

Alkyl/Glycosyl Sulfoxides as Radical Precursors and Their Use in the Synthesis of Pyridine Derivatives**

Xie, D., Wang, Y., Zhang, X., Fu, Z., & Niu, D. (2022) · Angewandte Chemie · doi:10.1002/ange.202204922 · Cited by 6

On the mechanism of deoxygenation of secondary alcohols by tin hydride reduction of methyl xanthates and other thiocarbonyl derivatives

Barton, D. H. R., Doo, O. J., & Jászberényi, J. C. (1990) · Tetrahedron Letters · doi:10.1016/s0040-4039(00)94480-0 · Cited by 74

ChemInform Abstract: On the Mechanism of Deoxygenation of Secondary Alcohols by Tin Hydride Reduction of Methyl Xanthates and Other Thiocarbonyl Derivatives.

Barton, D. H. R., Jang, D. O., & Jászberényi, J. C. (1991) · ChemInform · doi:10.1002/chin.199137101

On the mechanism of reduction of dithiocarbonates (xanthates) with tributylstannane

Barton, D. H. R., Crich, D., Löbberding, A., & Zard, S. Z. (1985) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39850000646 · Cited by 42

Studies of the mechanism of the reduction of different thioxanthen-9-ones

Kosińska, A., & Kinart, W. J. (2015) · Cogent Chemistry · doi:10.1080/23312009.2015.1064194

Reductions

Li, J. J., Limberakis, C., & Pflum, D. A. (2008) · Oxford University Press eBooks · doi:10.1093/oso/9780195187984.003.0010