| Year |
Citation |
Score |
| 2023 |
Quiclet-Sire B, Zard SZ. Some Aspects of α-(Acyloxy)alkyl Radicals in Organic Synthesis. Molecules (Basel, Switzerland). 28. PMID 38005282 DOI: 10.3390/molecules28227561 |
0.427 |
|
| 2023 |
Qiao H, Michalland J, Huang Q, Zard SZ. A Versatile Route to Acyl (MIDA)Boronates. Chemistry (Weinheim An Der Bergstrasse, Germany). e202302235. PMID 37477346 DOI: 10.1002/chem.202302235 |
0.453 |
|
| 2023 |
Quiclet-Sire B, Zard SZ. The xanthate route to tetralones, tetralins, and naphthalenes. A brief account. Organic & Biomolecular Chemistry. 21: 910-924. PMID 36607600 DOI: 10.1039/d2ob02159e |
0.377 |
|
| 2022 |
Bieszczad B, Chen X, Zard SZ. An Ionic-Radical Approach to Vicinally Functionalized Cyclopentanones and Cyclohexanones. Organic Letters. PMID 36534058 DOI: 10.1021/acs.orglett.2c03671 |
0.399 |
|
| 2022 |
Bieszczad B, Zard SZ. A Radical Route to α-Substituted Enones. Organic Letters. 24: 6973-6977. PMID 36129826 DOI: 10.1021/acs.orglett.2c02783 |
0.349 |
|
| 2022 |
Zeng X, Zard SZ. A Convergent Approach to 1,3-Dithiolan-2-ones and an Unexpected Synthesis of Lactones. Organic Letters. 24: 5245-5248. PMID 35861650 DOI: 10.1021/acs.orglett.2c02215 |
0.319 |
|
| 2022 |
Dorokhov VS, Quiclet-Sire B, Zard SZ. A Route to 5,5-Dithiospiroketals and to Long-Chain Monomers from the Biomass. Organic Letters. 24: 2878-2882. PMID 35404064 DOI: 10.1021/acs.orglett.2c00855 |
0.308 |
|
| 2022 |
Michalland J, Casaretto N, Zard SZ. A Modular Access to 1,2- and 1,3-Disubstituted Cyclobutylboronic Esters by Consecutive Radical Additions. Angewandte Chemie (International Ed. in English). 61: e202113333. PMID 34716652 DOI: 10.1002/anie.202113333 |
0.457 |
|
| 2021 |
Michalland J, Zard SZ. A Convergent, Stereoselective Route to Trisubstituted Alkenyl Boronates. Organic Letters. 23: 8018-8022. PMID 34617761 DOI: 10.1021/acs.orglett.1c03022 |
0.372 |
|
| 2020 |
Chen X, Zard SZ. Convergent Route to β-Amino Acids and to β-Heteroarylethylamines: An Unexpected Vinylation Reaction. Organic Letters. PMID 32314926 DOI: 10.1021/Acs.Orglett.0C01087 |
0.402 |
|
| 2020 |
Zard SZ. The Xanthate Route to Indolines, Indoles, and their Aza Congeners. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32314826 DOI: 10.1002/Chem.202001341 |
0.515 |
|
| 2020 |
Zard SZ. The Xanthate Route to Amino Acids. Chimia. 74: 9-17. PMID 32200781 DOI: 10.2533/Chimia.2020.9 |
0.413 |
|
| 2020 |
Zard SZ. The xanthate route to pyridines Tetrahedron. 76: 130802. DOI: 10.1016/J.Tet.2019.130802 |
0.532 |
|
| 2019 |
Lamb R, Revil-Baudard VL, Zard SZ. A Direct Approach to Orthogonally Protected α-Amino Aldehydes. Organic Letters. PMID 31343880 DOI: 10.1021/Acs.Orglett.9B02237 |
0.796 |
|
| 2019 |
Zard SZ, Huang Q, Michalland J. Alternating Radical Stabilities. Convergent Route to Terminal and Internal Boronates Qi Huang, Jean Michalland, and Samir Z. Zard. Angewandte Chemie (International Ed. in English). PMID 31243885 DOI: 10.1002/Ange.201906497 |
0.389 |
|
| 2019 |
Ostrovskis P, Mikhaylov AA, Zard SZ. Sigmatropic Rearrangement-Based Synthesis of 4-Alkenyl-1,3-dithiol-2-ones. Organic Letters. PMID 31025564 DOI: 10.1021/Acs.Orglett.9B01157 |
0.432 |
|
| 2019 |
Zard S. Sulfur Betaines from S-Propargyl Xanthates. Unusual Chemistry from a Simple Functional Group Synthesis. 51: 1006-1020. DOI: 10.1055/S-0037-1611638 |
0.457 |
|
| 2019 |
Quiclet-Sire B, Zard SZ. The xanthate route to all-carbon quaternary centers Science China-Chemistry. 62: 1450-1462. DOI: 10.1007/S11426-019-9587-X |
0.408 |
|
| 2019 |
Zard SZ. Radical Alliances: Solutions and Opportunities for Organic Synthesis Helvetica Chimica Acta. 102. DOI: 10.1002/Hlca.201900134 |
0.353 |
|
| 2018 |
Huang Q, Zard SZ. Radical Fragment Coupling Route to Geminal Bis(boronates). Organic Letters. PMID 30141953 DOI: 10.1021/Acs.Orglett.8B02235 |
0.452 |
|
| 2018 |
Zard SZ. The Xanthate Route to Ketones: When the Radical Is Better than the Enolate. Accounts of Chemical Research. PMID 29932322 DOI: 10.1021/Acs.Accounts.8B00201 |
0.534 |
|
| 2018 |
Revil-Baudard VL, Vors JP, Zard SZ. Xanthate-Mediated Incorporation of Quaternary Centers into Heteroarenes. Organic Letters. PMID 29856227 DOI: 10.1021/Acs.Orglett.8B01299 |
0.773 |
|
| 2018 |
Huang Q, Zard SZ. Inexpensive Radical Methylation and Related Alkylations of Heteroarenes. Organic Letters. PMID 29441790 DOI: 10.1021/Acs.Orglett.8B00190 |
0.38 |
|
| 2018 |
Zard S, Simonet-Davin R. A Direct Xanthate-Based Route to γ-Thiolactones Synlett. 29: 815-819. DOI: 10.1055/S-0036-1590987 |
0.481 |
|
| 2018 |
Huang Q, Qin L, Zard SZ. Xanthate-mediated intermolecular alkylation of pyrazines Tetrahedron. 74: 5804-5817. DOI: 10.1016/J.Tet.2018.08.040 |
0.436 |
|
| 2018 |
McCombie SW, Quiclet-Sire B, Zard SZ. Reflections on the mechanism of the Barton-McCombie Deoxygenation and on its consequences† Tetrahedron. 74: 4969-4979. DOI: 10.1016/J.Tet.2018.03.042 |
0.43 |
|
| 2017 |
Anthore-Dalion L, Zard SZ. Chemoselective Reduction: Xanthates as Traceless Precursors of Polyfunctionalized α,α-Dichloroketones. Organic Letters. PMID 28980470 DOI: 10.1021/Acs.Orglett.7B02636 |
0.78 |
|
| 2017 |
Braun MG, Castanedo G, Qin L, Salvo P, Zard SZ. Introduction of Trifluoroethylamine as Amide Isostere by C-H Functionalization of Heteroarenes. Organic Letters. PMID 28726421 DOI: 10.1021/Acs.Orglett.7B01880 |
0.37 |
|
| 2017 |
Huang Q, Zard SZ. Modular Route to Azaindanes. Organic Letters. PMID 28699347 DOI: 10.1021/Acs.Orglett.7B01772 |
0.483 |
|
| 2017 |
Quiclet-Sire B, Zard SZ. Some aspects of radical cascade and relay reactions. Proceedings. Mathematical, Physical, and Engineering Sciences. 473: 20160859. PMID 28484329 DOI: 10.1098/Rspa.2016.0859 |
0.404 |
|
| 2017 |
Mikhaylov AA, Zard SZ. Extension to the Silyl-Tethered Radical Cyclization: Cyclohex-2-en-1-oxy Vinyl Silanes in Stereoselective Radical Addition/Cyclization Cascades. Organic Letters. PMID 28358488 DOI: 10.1021/Acs.Orglett.7B00627 |
0.506 |
|
| 2017 |
Zard SZ. Radicals in Action: A Festival of Radical Transformations. The Journal of Organic Chemistry. 82: 2805. PMID 28301934 DOI: 10.1021/Acs.Joc.7B00431 |
0.387 |
|
| 2017 |
Quiclet-Sire B, Zard S. Convergent Routes to Pyrroles Exploiting the Unusual Radical Chemistry of Xanthates – An Overview Synlett. 28: 2685-2696. DOI: 10.1055/S-0036-1590809 |
0.52 |
|
| 2016 |
Anthore-Dalion L, Liu Q, Zard SZ. A Radical Bidirectional Fragment Coupling Route to Unsymmetrical Ketones. Journal of the American Chemical Society. PMID 27348440 DOI: 10.1021/Jacs.6B05344 |
0.814 |
|
| 2016 |
Zard SZ. The xanthate route to organofluorine derivatives. A brief account. Organic & Biomolecular Chemistry. PMID 27327241 DOI: 10.1039/C6Ob01087C |
0.447 |
|
| 2016 |
Li SG, Portela-Cubillo F, Zard SZ. A Convergent Synthesis of Enantiopure Open-Chain, Cyclic, and Fluorinated α-Amino Acids. Organic Letters. PMID 27054488 DOI: 10.1021/Acs.Orglett.6B00656 |
0.456 |
|
| 2016 |
Clemente-Tejeda D, Lara J, Zard S. A Direct Approach to Enantiopure Propionate Derivatives from Ethyl Lactate Synthesis. 48: 3393-3399. DOI: 10.1055/S-0035-1562449 |
0.377 |
|
| 2016 |
Quiclet-Sire B, Zard SZ. The Xanthate Route to Amines, Anilines, and Other Nitrogen Compounds. A Brief Account Synlett. 27: 680-701. DOI: 10.1055/S-0035-1561300 |
0.486 |
|
| 2016 |
Clemente-Tejeda D, Zard SZ. O -Ethyl- S -(1,2,2,2-Tetrafluoroethyl)-Dithiocarbonate: A Convenient Reagent for the Generation and Capture of 1,2,2,2-Tetra¯ fluoroethyl Radicals Synlett. 27: 136-140. DOI: 10.1055/S-0035-1560539 |
0.428 |
|
| 2016 |
Han S, Zard SZ. A convergent route to structures with multiple contiguous carbon–nitrogen bonds. The divergent role of N-acyl groups Tetrahedron. 72: 7859-7865. DOI: 10.1016/J.Tet.2016.05.085 |
0.373 |
|
| 2016 |
Boumediene M, Guignard RF, Zard SZ. Methoxycarbonyl migration in 3-methylene-1,4-cyclohexadienes. An extension of the von Auwers rearrangement Tetrahedron. 72: 3678-3686. DOI: 10.1016/J.Tet.2016.03.032 |
0.459 |
|
| 2016 |
Quiclet-Sire B, Zard SZ. On the Strategic Impact of the Degenerative Transfer of Xanthates on Synthetic Planning Israel Journal of Chemistry. 57: 202-217. DOI: 10.1002/Ijch.201600094 |
0.436 |
|
| 2015 |
Anthore L, Li S, White LV, Zard SZ. Radical Solution to the Alkylation of the Highly Base-Sensitive 1,1-Dichloroacetone. Application to the Synthesis of Z-Alkenoates and E,E-Dienoates. Organic Letters. 17: 5320-3. PMID 26457442 DOI: 10.1021/Acs.Orglett.5B02681 |
0.403 |
|
| 2015 |
Anthore L, Zard SZ. A Convergent Radical Based Route to Trifluoromethyl Ketones and to α,β-Unsaturated Trifluoromethyl Ketones. Organic Letters. 17: 3058-61. PMID 26057587 DOI: 10.1021/Acs.Orglett.5B01344 |
0.419 |
|
| 2015 |
Quiclet-Sire B, Zard SZ. Radical Instability in Aid of Efficiency: A Powerful Route to Highly Functional MIDA Boronates. Journal of the American Chemical Society. 137: 6762-5. PMID 25984592 DOI: 10.1021/Jacs.5B03893 |
0.457 |
|
| 2015 |
Debien L, Quiclet-Sire B, Zard SZ. Allylic alcohols: ideal radical allylating agents? Accounts of Chemical Research. 48: 1237-53. PMID 25905563 DOI: 10.1021/Acs.Accounts.5B00019 |
0.432 |
|
| 2015 |
Qin L, Zard SZ. Radical-based route to 2-(trifluoromethyl)-1,3,4-oxadiazoles and trifluoromethyl-substituted polycyclic 1,2,4-triazoles and dihydrofurans. Organic Letters. 17: 1577-80. PMID 25732871 DOI: 10.1021/Acs.Orglett.5B00457 |
0.528 |
|
| 2015 |
Qin L, Zard SZ. Radical-based route to 2-(trifluoromethyl)-1,3,4-oxadiazoles and trifluoromethyl -substituted polycyclic 1,2,4-triazoles and dihydrofurans Organic Letters. 17: 1577-1580. DOI: 10.1021/acs.orglett.5b00457 |
0.39 |
|
| 2015 |
Heng R, Zard SZ. A flexible route to substituted hydroxy-cyclopentanones from cyclobutanones Tetrahedron Letters. 56: 3679-3682. DOI: 10.1016/J.Tetlet.2015.04.063 |
0.434 |
|
| 2014 |
Li SG, Zard SZ. Novel route to triethylsilyl-substituted cyclopropanes. Organic Letters. 16: 6180-3. PMID 25415661 DOI: 10.1021/Ol503081B |
0.443 |
|
| 2014 |
Han S, Zard SZ. Stabilization of radicals by imides. A modular stereoselective approach to protected functional 1,2-diamines. Organic Letters. 16: 5386-9. PMID 25265571 DOI: 10.1021/Ol502599R |
0.46 |
|
| 2014 |
Salomon P, Zard SZ. A practical source of chlorodifluoromethyl radicals. Convergent routes to gem-difluoroalkenes and -dienes and (2,2-difluoroethyl)-indoles, -azaindoles, and -naphthols. Organic Letters. 16: 2926-9. PMID 24828527 DOI: 10.1021/Ol501063A |
0.433 |
|
| 2014 |
Qin L, Liu Z, Zard SZ. Carbon radical attack on a pyrimidine nitrogen. An unusual entry into polycyclic aminopyrimidones. Organic Letters. 16: 2966-9. PMID 24828397 DOI: 10.1021/Ol501104H |
0.438 |
|
| 2014 |
Liu Z, Qin L, Zard SZ. Radical ipso-substitution of a carbon-fluorine bond leading to fluoro-7-azaindolines and fluoro-7-azaindoles. Organic Letters. 16: 2704-7. PMID 24773583 DOI: 10.1021/Ol500985F |
0.408 |
|
| 2014 |
Quiclet-Sire B, Zard SZ. A radical thia-Brook rearrangement. Chemical Communications (Cambridge, England). 50: 5990-2. PMID 24763704 DOI: 10.1039/C4Cc01683A |
0.46 |
|
| 2014 |
Tran ND, Zard SZ. Convergent routes to substituted naphthylamides. Organic & Biomolecular Chemistry. 12: 3251-64. PMID 24733254 DOI: 10.1039/C4Ob00339J |
0.464 |
|
| 2014 |
Han S, Zard SZ. Modular approach to substituted Boc-protected 4-(Aminomethyl)pyrroles Organic Letters. 16: 1992-1995. PMID 24646397 DOI: 10.1021/Ol500544U |
0.498 |
|
| 2014 |
Salomon P, Zard SZ. A convergent route to geminal difluorosulfides and to functionalized difluorothiochromans, a new family of organofluorine compounds Organic Letters. 16: 1482-1485. PMID 24528287 DOI: 10.1021/Ol5002939 |
0.399 |
|
| 2014 |
Quiclet-Sire B, Yanagisawa Y, Zard SZ. A direct, versatile route to functionalized trialkoxysilanes. Chemical Communications (Cambridge, England). 50: 2324-6. PMID 24445860 DOI: 10.1039/C3Cc48570F |
0.42 |
|
| 2014 |
Jullien H, Quiclet-Sire B, Tétart T, Zard SZ. Flexible routes to thiophenes. Organic Letters. 16: 302-5. PMID 24299213 DOI: 10.1021/Ol403310F |
0.471 |
|
| 2014 |
Quiclet-Sire B, Zard SZ. A radical thia-Brook rearrangement Chemical Communications. 50: 5990-5992. DOI: 10.1039/c4cc01683a |
0.327 |
|
| 2014 |
Salomon P, Kosnik W, Zard SZ. A convergent, modular access to α-chloro-trifluoromethyl derivatives and to 1,1-difluoroalkenes Tetrahedron. DOI: 10.1016/J.Tet.2014.11.021 |
0.479 |
|
| 2014 |
Han S, Zard SZ. A convergent route to substituted azetidines and to Boc-protected 4-aminomethylpyrroles Tetrahedron. DOI: 10.1016/J.Tet.2014.10.054 |
0.506 |
|
| 2014 |
Han S, Jones RA, Quiclet-Sire B, Zard SZ. A convergent route to functional protected amines, diamines, and β-amino acids Tetrahedron. DOI: 10.1016/J.Tet.2014.07.055 |
0.473 |
|
| 2013 |
Debien L, Braun MG, Quiclet-Sire B, Zard SZ. Tri- and tetrasubstituted functionalized vinyl sulfides by radical allylation. Organic Letters. 15: 6250-3. PMID 24266882 DOI: 10.1021/Ol403103U |
0.541 |
|
| 2013 |
Debien L, Zard SZ. A two-step synthesis of α-keto vinyl carbinols from ketones. Organic Letters. 15: 6066-9. PMID 24215234 DOI: 10.1021/Ol4029594 |
0.431 |
|
| 2013 |
Quiclet-Sire B, Zard SZ. An expedient route to dihydrothiazines, a virtually unknown class of heterocycles Organic Letters. 15: 5886-5889. PMID 24199993 DOI: 10.1021/Ol402973Q |
0.341 |
|
| 2013 |
Li SG, Zard SZ. A convenient metal-free reagent for the generation and capture of trifluoromethanethiol. Organic Letters. 15: 5898-901. PMID 24191718 DOI: 10.1021/Ol403038F |
0.363 |
|
| 2013 |
Goh KK, Kim S, Zard SZ. A synthesis of (1E,3E)-TMS dienes from keto-xanthates via Chugaev-type elimination. The Journal of Organic Chemistry. 78: 12274-9. PMID 24180486 DOI: 10.1021/Jo402169V |
0.313 |
|
| 2013 |
Goh KK, Kim S, Zard SZ. Free-radical variant for the synthesis of functionalized 1,5-diketones. Organic Letters. 15: 4818-21. PMID 24011200 DOI: 10.1021/Ol402213K |
0.48 |
|
| 2013 |
Guignard RF, Petit L, Zard SZ. A method for the net contra-thermodynamic isomerization of cyclic trisubstituted alkenes Organic Letters. 15: 4178-4181. PMID 23924355 DOI: 10.1021/Ol4018744 |
0.402 |
|
| 2013 |
Quiclet-Sire B, Zard SZ. Some aspects of radical chemistry in the assembly of complex molecular architectures. Beilstein Journal of Organic Chemistry. 9: 557-76. PMID 23616797 DOI: 10.3762/Bjoc.9.61 |
0.38 |
|
| 2013 |
Debien L, Zard SZ. From a remarkable manifestation of polar effects in a radical fragmentation to the convergent synthesis of highly functionalized ketones Journal of the American Chemical Society. 135: 3808-3811. PMID 23425262 DOI: 10.1021/Ja400831W |
0.519 |
|
| 2013 |
Goh KKK, Kim S, Zard SZ. Free-radical variant for the synthesis of functionalized 1,5-diketones Organic Letters. 15: 4818-4821. DOI: 10.1021/ol402213k |
0.335 |
|
| 2012 |
Liu Z, Qin L, Zard SZ. Expedient approach to novel N-unprotected bicyclic azapyrimidine and pyridine structures Organic Letters. 14: 5976-5979. PMID 23167272 DOI: 10.1021/Ol3028829 |
0.41 |
|
| 2012 |
Quiclet-Sire B, Tran ND, Zard SZ. An unusual synthesis of N-unsubstituted benzazepinones. Organic Letters. 14: 5514-7. PMID 23078051 DOI: 10.1021/Ol3026044 |
0.361 |
|
| 2012 |
Quiclet-Sire B, Zard SZ. Some aspects of the radical chemistry of xanthates Chimia. 66: 404-412. PMID 22871284 DOI: 10.2533/Chimia.2012.404 |
0.478 |
|
| 2012 |
Charrier N, Liu Z, Zard SZ. Desulfonylative radical ring closure onto aromatics. A modular route to benzazepin-2-ones and 5-arylpiperidin-2-ones Organic Letters. 14: 2018-2021. PMID 22463494 DOI: 10.1021/Ol3005276 |
0.46 |
|
| 2012 |
El Qacemi M, Petit L, Quiclet-Sire B, Zard SZ. A unified access to diverse heteroaromatic scaffolds using the radical chemistry of xanthates Organic and Biomolecular Chemistry. 10: 5707-5719. PMID 22434284 DOI: 10.1039/C2Ob25169H |
0.453 |
|
| 2012 |
Hawkins B, Paddock VL, Tölle N, Zard SZ. A convenient conversion of terminal alkenes into homologous unsaturated and doubly unsaturated esters. Organic Letters. 14: 1020-3. PMID 22296044 DOI: 10.1021/Ol203387R |
0.73 |
|
| 2012 |
Bacque E, Qacemi ME, Zard SZ. A Flexible Convergent Route to Azaoxindoles, Azaindolines, Azaindoles, and Tetrahydroazaquinolones Heterocycles. 84: 291-299. DOI: 10.3987/Com-11-S(P)24 |
0.51 |
|
| 2012 |
Revol G, Fuchs C, Zard SZ. A short formal total synthesis of (±)-hirsutic acid Canadian Journal of Chemistry. 90: 927-931. DOI: 10.1139/V2012-037 |
0.459 |
|
| 2012 |
Hawkins B, Paddock VL, Tölle N, Zard SZ. A convenient conversion of terminal alkenes into homologous unsaturated and doubly unsaturated esters Organic Letters. 14: 1020-1023. DOI: 10.1021/ol203387r |
0.703 |
|
| 2012 |
Petit L, Botez I, Tizot A, Zard SZ. A flexible radical approach to 5-substituted 4,5-dihydro-3H-pyrido[4,3-b] azepin-2-ones. Some mechanistic observations on the radical cyclisation- aromatisation process Tetrahedron Letters. 53: 3220-3224. DOI: 10.1016/J.Tetlet.2012.04.020 |
0.476 |
|
| 2012 |
Zard SZ. Some intriguing mechanistic aspects of the radical chemistry of xanthates Journal of Physical Organic Chemistry. 25: 953-964. DOI: 10.1002/Poc.2976 |
0.413 |
|
| 2012 |
Zard SZ. Some aspects of the chemistry of nitro compounds Helvetica Chimica Acta. 95: 1730-1757. DOI: 10.1002/Hlca.201200324 |
0.456 |
|
| 2012 |
Petit L, Botez I, Tizot A, Zard SZ. ChemInform Abstract: A Flexible Radical Approach to 5-Substituted 4,5-Dihydro-3H-pyrido[4,3-b]azepin-2-ones. Some Mechanistic Observations on the Radical Cyclization-Aromatization Process. Cheminform. 43: no-no. DOI: 10.1002/chin.201242181 |
0.337 |
|
| 2012 |
Charrier N, Liu Z, Zard SZ. ChemInform Abstract: Desulfonylative Radical Ring Closure onto Aromatics. A Modular Route to Benzazepin-2-ones and 5-Arylpiperidin-2-ones. Cheminform. 43: no-no. DOI: 10.1002/chin.201234159 |
0.374 |
|
| 2011 |
Brioche J, Michalak M, Quiclet-Sire B, Zard SZ. Elimination versus ring opening: a convergent route to alkylidene-cyclobutanes. Organic Letters. 13: 6296-9. PMID 22070865 DOI: 10.1021/Ol202798R |
0.81 |
|
| 2011 |
Guignard RF, Zard SZ. A convergent approach to polycyclic aromatic hydrocarbons Chemical Communications. 47: 12185-12187. PMID 21998824 DOI: 10.1039/C1Cc15095B |
0.441 |
|
| 2011 |
Debien L, Quiclet-Sire B, Zard SZ. Modular approach to saturated and α,β-unsaturated ketones. Organic Letters. 13: 5676-9. PMID 21954958 DOI: 10.1021/Ol202399C |
0.447 |
|
| 2011 |
Braun MG, Quiclet-Sire B, Zard SZ. A highly stereoselective, modular route to (E)-vinylsulfones and to (Z)- and (E)-alkenes. Journal of the American Chemical Society. 133: 15954-7. PMID 21923183 DOI: 10.1021/Ja207944C |
0.341 |
|
| 2011 |
Quiclet-Sire B, Tölle N, Zafar SN, Zard SZ. Oxime derivatives as α-electrophiles. from α-tetralone oximes to tetracyclic frameworks. Organic Letters. 13: 3266-9. PMID 21615103 DOI: 10.1021/Ol2012204 |
0.45 |
|
| 2011 |
Heng R, Zard SZ. A flexible, unified radical-based approach to polycyclic structures. Organic & Biomolecular Chemistry. 9: 3396-404. PMID 21423942 DOI: 10.1039/C1Ob00024A |
0.424 |
|
| 2011 |
Braun MG, Heng R, Zard SZ. Transfer of chirality by the use of an all carbon tether. Organic Letters. 13: 1230-3. PMID 21288011 DOI: 10.1021/Ol2001182 |
0.404 |
|
| 2011 |
Heng R, Zard SZ. Access to 1,2-diketones by an unusual radical cascade Chemical Communications. 47: 3296-3298. PMID 21283911 DOI: 10.1039/C0Cc04725B |
0.394 |
|
| 2011 |
Braun MG, Zard SZ. An approach to α-keto vinyl carbinols. Organic Letters. 13: 776-9. PMID 21244049 DOI: 10.1021/Ol103044X |
0.459 |
|
| 2011 |
Quiclet-Sire B, Zard SZ. Fun with radicals: Some new perspectives for organic synthesis Pure and Applied Chemistry. 83: 519-551. DOI: 10.1351/Pac-Con-10-08-07 |
0.427 |
|
| 2011 |
Laot Y, Petit L, Tran NDM, Zard SZ. Fluoroazaindolines by an uncommon radical ipso-substitution of a C-F bond Australian Journal of Chemistry. 64: 416-425. DOI: 10.1071/Ch10422 |
0.457 |
|
| 2011 |
Li Z, Alameda-Angulo C, Quiclet-Sire B, Zard SZ. A flexible approach to hexahydronaphthalene-1-carboxylates Tetrahedron. 67: 9844-9852. DOI: 10.1016/J.Tet.2011.09.103 |
0.331 |
|
| 2010 |
Laot Y, Petit L, Zard SZ. Synthesis of fluoroazaindolines by an uncommon radical ipso substitution of a carbon-fluorine bond. Organic Letters. 12: 3426-9. PMID 20670008 DOI: 10.1021/Ol101240F |
0.457 |
|
| 2010 |
Laot Y, Petit L, Zard SZ. Unusual radical addition on a heteroaromatic nitrogen. A convenient access to new pyrimidine derivatives. Chemical Communications (Cambridge, England). 46: 5784-6. PMID 20574573 DOI: 10.1039/C0Cc00533A |
0.444 |
|
| 2010 |
Petit L, Zard SZ. A radical-based approach to hydroxytetralones from unprotected phenols. Chemical Communications (Cambridge, England). 46: 5148-50. PMID 20552133 DOI: 10.1039/C0Cc00680G |
0.491 |
|
| 2010 |
Dias-Jurberg I, Gagosz F, Zard SZ. Unusual approach to branched 3-alkynylamides and to 1,5-dihydropyrrol-2-ones. Organic Letters. 12: 416-9. PMID 20067299 DOI: 10.1021/Ol902472R |
0.42 |
|
| 2010 |
Quiclet-Sire B, Zard SZ. A convenient, high yielding cleavage of the thiocarbonyl group in xanthates Bulletin of the Korean Chemical Society. 31: 543-544. DOI: 10.5012/Bkcs.2010.31.03.543 |
0.312 |
|
| 2010 |
Quiclet-Sire B, Zard SZ. A flexible route to 4-substituted β-lactams Heterocycles. 82: 263-271. DOI: 10.3987/Com-10-S(E)39 |
0.501 |
|
| 2010 |
Laot Y, Petit L, Zard SZ. Unusual radical addition on a heteroaromatic nitrogen. A convenient access to new pyrimidine derivatives Chemical Communications. 46: 5784-5786. DOI: 10.1039/c0cc00533a |
0.364 |
|
| 2010 |
Laot Y, Petit L, Zard SZ. Synthesis of fluoroazaindolines by an uncommon radical ipso substitution of a carbon-fluorine bond Organic Letters. 12: 3426-3429. DOI: 10.1021/ol101240f |
0.312 |
|
| 2010 |
Boutillier P, Quiclet-Sire B, Zafar SN, Zard SZ. A divergent approach to highly substituted benzothiepinones and to 2,3-dihydrothieno[2,3-b]thiopyran-4-ones Tetrahedron Asymmetry. 21: 1649-1665. DOI: 10.1016/J.Tetasy.2010.06.006 |
0.403 |
|
| 2010 |
Quiclet-Sire B, Revol G, Zard SZ. A convergent, modular access to complex amines Tetrahedron. 66: 6656-6666. DOI: 10.1016/J.Tet.2010.05.107 |
0.39 |
|
| 2010 |
LY T, LASO NM, ZARD SZ. ChemInform Abstract: A New Synthesis of 3-Aryl Substituted Oxindoles. Cheminform. 29: no-no. DOI: 10.1002/chin.199831110 |
0.31 |
|
| 2010 |
LE GUYADER F, QUICLET-SIRE B, SEGUIN S, ZARD SZ. ChemInform Abstract: New Radical Allylation Reaction of Iodides. Cheminform. 28: no-no. DOI: 10.1002/chin.199748070 |
0.354 |
|
| 2010 |
QUICLET-SIRE B, SAICIC RN, ZARD SZ. ChemInform Abstract: A Convenient Synthesis of Trifluoromethyl Aryl Sulfides. Cheminform. 28: no-no. DOI: 10.1002/chin.199715092 |
0.304 |
|
| 2010 |
DENIEUL M, QUICLET-SIRE B, ZARD SZ. ChemInform Abstract: Trifluoroacetonyl Radicals: A Versatile Approach to Trifluoromethyl Ketones. Cheminform. 28: no-no. DOI: 10.1002/chin.199713055 |
0.353 |
|
| 2010 |
QUICLET-SIRE B, SAUNIER J, ZARD SZ. ChemInform Abstract: β-Lactams by a Nickel Powder/Acetic Acid Mediated Radical Cyclization. Cheminform. 27: no-no. DOI: 10.1002/chin.199624132 |
0.308 |
|
| 2010 |
QUICLET-SIRE B, ZARD SZ. ChemInform Abstract: New Radical Allylation Reaction. Cheminform. 27: no-no. DOI: 10.1002/chin.199624086 |
0.349 |
|
| 2010 |
AXON J, BOITEAU L, BOIVIN J, FORBES JE, ZARD SZ. ChemInform Abstract: A New Radical-Based Synthesis of Lactams and Indolones from Dithiocarbonates (Xanthates). Cheminform. 25: no-no. DOI: 10.1002/chin.199434074 |
0.369 |
|
| 2010 |
BOIVIN J, FOUQUET E, ZARD SZ. ChemInform Abstract: Iminyl Radicals. Part 2. Ring Opening of Cyclobutyl- and Cyclopentyliminyl Radicals. Cheminform. 25: no-no. DOI: 10.1002/chin.199422080 |
0.361 |
|
| 2010 |
BOIVIN J, FOUQUET E, ZARD SZ. ChemInform Abstract: Iminyl Radicals. Part 1. Generation and Intramolecular Capture by an Olefin. Cheminform. 25: no-no. DOI: 10.1002/chin.199422079 |
0.352 |
|
| 2010 |
BARTON DHR, GATEAU-OLESKER A, GERO SD, LACHER B, TACHDJIAN C, ZARD SZ. ChemInform Abstract: Radical Decarboxylative Alkylation of Tartaric Acid. Cheminform. 24: no-no. DOI: 10.1002/chin.199339123 |
0.346 |
|
| 2010 |
BARTON DHR, BOIVIN J, CREPON E, SARMA J, TOGO H, ZARD SZ. ChemInform Abstract: Decarboxylative Radical Addition to Vinylsulfones and Vinylphosphonium Bromide: Some Further Novel Transformations of Geminal (Pyridine-2- thiyl) Phenylsulfones. Cheminform. 22: no-no. DOI: 10.1002/chin.199151195 |
0.323 |
|
| 2009 |
Quiclet-Sire B, Revol G, Zard SZ. Functional primary amines and diamines from α-aminoacids. A concise route to substituted 2-aminotetralins Organic Letters. 11: 3554-3557. PMID 19610605 DOI: 10.1021/Ol901263T |
0.504 |
|
| 2009 |
Lebreux F, Quiclet-Sire B, Zard SZ. Radical arylaminomethylation of unactivated alkenes. Organic Letters. 11: 2844-7. PMID 19507839 DOI: 10.1021/Ol901055J |
0.452 |
|
| 2009 |
Li Z, Zard SZ. A flexible radical-based approach to TMS-substituted propargyl alcohols and to 2,3-allenols. Organic Letters. 11: 2868-71. PMID 19507838 DOI: 10.1021/Ol900739X |
0.405 |
|
| 2009 |
Quiclet-Sire B, Revol G, Zard SZ. A convergent radical-based route to biaryls Organic Letters. 11: 2832-2835. PMID 19492807 DOI: 10.1021/Ol9010294 |
0.447 |
|
| 2009 |
Blechy A, Zard SZ. A flexible, convergent approach to polycyclic indole structures: Formal synthesis of (±)-mersicarpine Organic Letters. 11: 2800-2803. PMID 19489601 DOI: 10.1021/Ol900996K |
0.5 |
|
| 2009 |
Zard SZ. The art of the soluble: Synthetic problems from industry as a springboard for the discovery of new chemical reactions Synlett. 333-353. DOI: 10.1055/S-0028-1087546 |
0.371 |
|
| 2009 |
Lebreux F, Quiclet-Sire B, Zard SZ. Radical arylaminomethylation of unactivated alkenes Organic Letters. 11: 2844-2847. DOI: 10.1021/ol901055j |
0.335 |
|
| 2009 |
Li Z, Zard SZ. A flexible, modular route to cyclopentanols Tetrahedron Letters. 50: 6973-6976. DOI: 10.1016/J.Tetlet.2009.09.157 |
0.448 |
|
| 2009 |
Heng R, Quiclet-Sire B, Zard SZ. Substitution of chlorocyclobutanones with xanthate salts. The remarkable effect of added base Tetrahedron Letters. 50: 3613-3616. DOI: 10.1016/J.Tetlet.2009.03.133 |
0.389 |
|
| 2009 |
Biechy A, Hachisu S, Quiclet-Sire B, Ricard L, Zard SZ. Application of an amidyl radical cascade to the total synthesis of (±)-fortucine leading to the structural revision of kirkine Tetrahedron. 65: 6730-6738. DOI: 10.1016/J.Tet.2009.04.027 |
0.401 |
|
| 2008 |
Charrier N, Zard SZ. Radical allylation with alpha-branched allyl sulfones. Angewandte Chemie (International Ed. in English). 47: 9443-6. PMID 18979487 DOI: 10.1002/Anie.200804298 |
0.425 |
|
| 2008 |
Zard SZ. Recent progress in the generation and use of nitrogen-centred radicals. Chemical Society Reviews. 37: 1603-18. PMID 18648685 DOI: 10.1039/B613443M |
0.384 |
|
| 2008 |
Corbet M, Ferjančić Z, Quiclet-Sire B, Zard SZ. Radical, one-step approach to o-chlorophenyl thioethers from xanthates. A rapid access to vinylsilanes Organic Letters. 10: 3579-3582. PMID 18646770 DOI: 10.1021/Ol801348U |
0.418 |
|
| 2008 |
Quiclet-Sire B, Zard SZ. Radical aminomethylation of unactivated alkenes. Organic Letters. 10: 3279-82. PMID 18582076 DOI: 10.1021/Ol801162M |
0.408 |
|
| 2008 |
Charrier N, Quiclet-Sire B, Zard SZ. Allylic alcohols as radical allylating agents. An overall olefination of aldehydes and ketones. Journal of the American Chemical Society. 130: 8898-9. PMID 18558685 DOI: 10.1021/Ja802899M |
0.364 |
|
| 2008 |
Corbet M, Zard SZ. Facile and efficient one-pot synthesis of highly functionalized thieno[2,3-b]thiopyran-4-ones from beta-keto epsilon-xanthyl phosphonates. Organic Letters. 10: 2861-4. PMID 18529013 DOI: 10.1021/Ol801033E |
0.38 |
|
| 2008 |
Corbet M, De Greet M, Zard SZ. A highly conjunctive β-keto phosphonate: Application to the synthesis of pyridine alkaloids xestamines C, E, and H Organic Letters. 10: 253-256. PMID 18161980 DOI: 10.1021/Ol702590F |
0.393 |
|
| 2008 |
Ferjancic Z, Quiclet-Sire B, Zard SZ. Generation and intermodular additions of pyridylmethyl radicals Synthesis. 2996-3008. DOI: 10.1055/S-2008-1067198 |
0.503 |
|
| 2008 |
Quiclet-Sire B, Zard SZ. Radical aminomethylation of unactivated alkenes Organic Letters. 10: 3279-3282. DOI: 10.1021/ol801162m |
0.338 |
|
| 2008 |
Quiclet-Sire B, Woollaston D, Zard SZ. A versatile radical based approach to O-alkylated hydroxylamines and oximes Tetrahedron. 64: 11917-11924. DOI: 10.1016/J.Tet.2008.08.113 |
0.363 |
|
| 2008 |
Callier-Dublanchet AC, Cassayre J, Gagosz F, Quiclet-Sire B, Sharp LA, Zard SZ. Amidyls in radical cascades. The total synthesis of (±)-aspidospermidine and (±)-13-deoxyserratine Tetrahedron. 64: 4803-4816. DOI: 10.1016/J.Tet.2008.02.107 |
0.371 |
|
| 2008 |
Callier-Dublanchet A, Cassayre J, Gagosz F, Quiclet-Sire B, Sharp LA, Zard SZ. ChemInform Abstract: Amidyls in Radical Cascades. The Total Synthesis of (.+-.)-Aspidospermidine (III) and (.+-.)-13-Deoxyserratine (Vb). Cheminform. 39. DOI: 10.1002/chin.200839200 |
0.354 |
|
| 2008 |
Charrier N, Zard SZ. Radical allylation with α-branched allyl sulfones Angewandte Chemie - International Edition. 47: 9443-9446. DOI: 10.1002/anie.200804298 |
0.346 |
|
| 2007 |
De Greet M, Zard SZ. Unified, radical-based approach for the synthesis of spiroketals Organic Letters. 9: 1773-1776. PMID 17391041 DOI: 10.1021/Ol070488+ |
0.511 |
|
| 2007 |
Zard SZ. New routes to organofluorine compounds based on ketenes and the radical transfer of xanthates Organic and Biomolecular Chemistry. 5: 205-213. PMID 17205160 DOI: 10.1039/B615592H |
0.446 |
|
| 2007 |
Mougin C, Sançon J, Zard SZ. A practical route to pyrazines and quinoxalines, and an unusual synthesis of benzimidazoles Heterocycles. 74: 211-218. DOI: 10.3987/Com-07-S(W)55 |
0.452 |
|
| 2007 |
Zard S, Qacemi M, Ricard L. Radical-Mediated Synthesis of Imidazopyridinones Synfacts. 2007: 0138-0138. DOI: 10.1055/s-2006-955821 |
0.377 |
|
| 2007 |
Gheorghe A, Quiclet-Sire B, Vila X, Zard SZ. Synthesis of substituted 3-arylpiperidines and 3-arylpyrrolidines by radical 1,4 and 1,2-aryl migrations Tetrahedron. 63: 7187-7212. DOI: 10.1016/J.Tet.2007.04.091 |
0.521 |
|
| 2007 |
Zard SZ. Syntheses of organofluorine derivatives by a new radical process Acs Symposium Series. 949: 25-38. |
0.307 |
|
| 2006 |
Fabre S, Vila X, Zard SZ. An unexpected synthesis of ketene monothioacetals Chemical Communications. 4964-4966. PMID 17136262 DOI: 10.1039/B612336H |
0.35 |
|
| 2006 |
El-Qacemi M, Ricard L, Zard SZ. An unprecedented radical ring closure on a pyridine nitrogen. Chemical Communications (Cambridge, England). 4422-4. PMID 17057864 DOI: 10.1039/B609021D |
0.45 |
|
| 2006 |
Charrier N, Gravestock D, Zard SZ. Radical additions of xanthates to vinyl epoxides and related derivatives: a powerful tool for the modular creation of quaternary centers. Angewandte Chemie (International Ed. in English). 45: 6520-3. PMID 16972293 DOI: 10.1002/Anie.200601567 |
0.391 |
|
| 2006 |
Ouvry G, Quiclet-Sire B, Zard SZ. Substituted allyl diphenylphosphine oxides as radical allylating agents. Angewandte Chemie (International Ed. in English). 45: 5002-6. PMID 16856202 DOI: 10.1002/Anie.200601556 |
0.45 |
|
| 2006 |
Quiclet-Sire B, Zard SZ. Powerful carbon - Carbon bond forming reactions based on a novel radical exchange process Chemistry - a European Journal. 12: 6002-6016. PMID 16791885 DOI: 10.1002/Chem.200600510 |
0.489 |
|
| 2006 |
Cordero-Vargas A, Quiclet-Sire B, Zard SZ. A flexible approach for the preparation of substituted benzazepines: Application to the synthesis of tolvaptan Bioorganic and Medicinal Chemistry. 14: 6165-6173. PMID 16782344 DOI: 10.1016/J.Bmc.2006.05.070 |
0.415 |
|
| 2006 |
Coote ML, Easton CJ, Zard SZ. Factors affecting the relative and absolute rates of beta-scission of alkoxythiocarbonyl radicals and alkoxycarbonyl radicals. The Journal of Organic Chemistry. 71: 4996-9. PMID 16776533 DOI: 10.1021/Jo0607313 |
0.397 |
|
| 2006 |
Quiclet-Sire B, Zard SZ. Observations on the reaction of hydrazones with iodine: interception of the diazo intermediates. Chemical Communications (Cambridge, England). 1831-2. PMID 16622498 DOI: 10.1039/B602580C |
0.376 |
|
| 2006 |
Sharp LA, Zard SZ. A short total synthesis of (+/-)-aspidospermidine. Organic Letters. 8: 831-4. PMID 16494452 DOI: 10.1021/Ol052749Q |
0.502 |
|
| 2006 |
Guindeuil S, Zard SZ. An unusual approach to spirolactones and related structures. Chemical Communications (Cambridge, England). 665-7. PMID 16446845 DOI: 10.1039/B516020K |
0.419 |
|
| 2006 |
Bergeot O, Corsi C, El Qacemi M, Zard SZ. S-(3-Chloro-2-oxo-propyl)-O-ethyl xanthate: a linchpin radical coupling agent for the synthesis of heterocyclic and polycyclic compounds. Organic & Biomolecular Chemistry. 4: 278-90. PMID 16391770 DOI: 10.1039/B514509K |
0.388 |
|
| 2006 |
Bagal SK, de Greef M, Zard SZ. Cyano(ethoxycarbonothioylthio)methyl benzoate: a novel one-carbon radical equivalent. Organic Letters. 8: 147-50. PMID 16381589 DOI: 10.1021/Ol052634M |
0.441 |
|
| 2006 |
Vila X, Zard SZ. Synthesis of substituted 4-arylpiperidin-2-ones by a 6-exo-trig radical cyclization Heterocycles. 70: 45-50. DOI: 10.3987/Com-06-S(W)7 |
0.513 |
|
| 2006 |
Zard SZ. The genesis of the reversible radical addition-fragmentation-transfer of thiocarbonylthio derivatives from the Barton-McCombie deoxygenation: A brief account and some mechanistic observations Australian Journal of Chemistry. 59: 663-668. DOI: 10.1071/Ch06263 |
0.368 |
|
| 2006 |
Bagal SK, Tournier L, Zard SZ. Radicals from aldehydes: A convergent access to dienes and δ-lactones Synlett. 1485-1490. DOI: 10.1055/S-2006-941582 |
0.466 |
|
| 2006 |
Qacemi ME, Ricard L, Zard SZ. An unprecedented radical ring closure on a pyridine nitrogen Chemical Communications. 4422-4424. DOI: 10.1039/b609021d |
0.348 |
|
| 2006 |
Alameda-Angulo C, Quiclet-Sire B, Zard SZ. An expedient approach to allenes and polycyclic structures using propargyl radicals Tetrahedron Letters. 47: 913-916. DOI: 10.1016/J.Tetlet.2005.11.154 |
0.457 |
|
| 2006 |
Gagosz F, Zard SZ. A Xanthate‐Transfer Approach to α‐Trifluoromethylamines [2‐(N‐Acetylamino)‐4,4‐Dimethoxy‐1,1,1‐Trifluorobutane] Organic Syntheses. 84: 32-42. DOI: 10.1002/0471264229.Os084.04 |
0.375 |
|
| 2005 |
Cordero-Vargas A, Quiclet-Sire B, Zard SZ. Model studies towards the synthesis of gilvocarcin M. Organic & Biomolecular Chemistry. 3: 4432-43. PMID 16327904 DOI: 10.1039/B512851J |
0.363 |
|
| 2005 |
Heinrich MR, Pérez-Martín I, Zard SZ. Generation and ring opening of aziridine N-carbonyl radicals. Chemical Communications (Cambridge, England). 5928-30. PMID 16317478 DOI: 10.1039/b512956g |
0.336 |
|
| 2005 |
Bacqué E, El Qacemi M, Zard SZ. An unusual radical Smiles rearrangement. Organic Letters. 7: 3817-20. PMID 16092883 DOI: 10.1021/Ol051568L |
0.445 |
|
| 2005 |
Alameda-Angulo C, Quiclet-Sire B, Schmidt E, Zard SZ. On the [2,3] sigmatropic rearrangement of allylic nitro compounds. Organic Letters. 7: 3489-92. PMID 16048324 DOI: 10.1021/Ol051196G |
0.366 |
|
| 2005 |
Heinrich MR, Sharp LA, Zard SZ. A convergent approach to gamma-carbonyl vinyl boronates. Chemical Communications (Cambridge, England). 3077-9. PMID 15959590 DOI: 10.1039/B502885J |
0.426 |
|
| 2005 |
Gheorghe A, Quiclet-Sire B, Vila X, Zard SZ. Synthesis of 3-arylpiperidines by a radical 1,4-aryl migration. Organic Letters. 7: 1653-6. PMID 15816775 DOI: 10.1021/Ol0503642 |
0.512 |
|
| 2005 |
Barclay GL, Quiclet-Sire B, Sanchez-Jimenez G, Zard SZ. Model studies toward the synthesis of kirkine. Organic & Biomolecular Chemistry. 3: 823-35. PMID 15731869 DOI: 10.1039/B416763E |
0.469 |
|
| 2005 |
Quiclet-Sire B, Zard SZ. The synthesis of 1,2,3-triazoles from nitroalkenes - Revisited Synthesis. 3319-3326. DOI: 10.1055/S-2005-918463 |
0.453 |
|
| 2005 |
Briggs ME, Zard SZ. A new radical-ionic allylation sequence Synlett. 334-336. DOI: 10.1055/S-2004-837191 |
0.477 |
|
| 2005 |
Binot G, Zard SZ. Access to 4-substituted 3,4-dihydroquinolin-2(1H)-ones by an unusual radical cyclisation of a secondary amide Tetrahedron Letters. 46: 7503-7506. DOI: 10.1016/J.Tetlet.2005.09.006 |
0.428 |
|
| 2005 |
Tournier L, Zard SZ. A practical variation on the Leuckart reaction Tetrahedron Letters. 46: 971-973. DOI: 10.1016/J.Tetlet.2004.12.042 |
0.464 |
|
| 2005 |
Tournier L, Zard SZ. A direct approach to α-hydroxy and α-chloro trifluoromethyl derivatives Tetrahedron Letters. 46: 455-459. DOI: 10.1016/J.Tetlet.2004.11.086 |
0.475 |
|
| 2004 |
Heinrich MR, Zard SZ. Generation and intermolecular capture of cyclopropylacyl radicals. Organic Letters. 6: 4969-72. PMID 15606112 DOI: 10.1021/Ol047892I |
0.474 |
|
| 2004 |
Cordero-Vargas A, Perez-Martin I, Quiclet-Sire B, Zard SZ. Synthesis of substituted naphthalenes from alpha-tetralones generated by a xanthate radical addition-cyclisation sequence. Organic & Biomolecular Chemistry. 2: 3018-25. PMID 15480467 DOI: 10.1039/B411158C |
0.406 |
|
| 2004 |
Bacqué E, El Qacemi M, Zard SZ. Tin-free radical cyclizations for the synthesis of 7-azaoxindoles, 7-azaindolines, tetrahydro[1,8]naphthyridines, and tetrahydro-5H-pyrido[2,3-b]azepin-8-ones. Organic Letters. 6: 3671-4. PMID 15469320 DOI: 10.1021/Ol0489649 |
0.479 |
|
| 2004 |
Moutrille C, Zard SZ. A new, practical access to amidyl radicals. Chemical Communications (Cambridge, England). 1848-9. PMID 15306914 DOI: 10.1039/B405545D |
0.398 |
|
| 2004 |
Cordero-Vargas A, Quiclet-Sire B, Zard SZ. A new access to C-arylglycosides related to the gilvocarcins Tetrahedron Letters. 45: 7335-7338. DOI: 10.1016/J.Tetlet.2004.08.009 |
0.393 |
|
| 2004 |
Briggs ME, El Qacemi M, Kalaï C, Zard SZ. A new approach to the synthesis of polycyclic structures Tetrahedron Letters. 45: 6017-6020. DOI: 10.1016/J.Tetlet.2004.06.035 |
0.448 |
|
| 2004 |
Moutrille C, Zard SZ. A new approach for the ortho-substitution of anilines and for the synthesis of indolines Tetrahedron Letters. 45: 4631-4634. DOI: 10.1016/J.Tetlet.2004.04.111 |
0.447 |
|
| 2004 |
De Greef M, Zard SZ. Xanthates derived from 1,3-dithiane and its monosulfoxide; one-carbon radical equivalents Tetrahedron. 60: 7781-7791. DOI: 10.1016/J.Tet.2004.06.061 |
0.482 |
|
| 2003 |
Vargas AC, Quiclet-Sire B, Zard SZ. Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence. Organic Letters. 5: 3717-9. PMID 14507213 DOI: 10.1021/Ol035394O |
0.388 |
|
| 2003 |
Gennet D, Zard SZ, Zhang H. Amidinyl radicals: new and useful intermediates for the synthesis of imidazolines and imidazoles. Chemical Communications (Cambridge, England). 1870-1. PMID 12932008 DOI: 10.1039/B304545E |
0.467 |
|
| 2003 |
Ouvry G, Quiclet-Sire B, Zard SZ. beta-Nitro xanthates as olefin precursors. Organic Letters. 5: 2907-9. PMID 12889905 DOI: 10.1021/Ol035027C |
0.309 |
|
| 2003 |
Gagosz F, Zard SZ. A direct approach to alpha-trifluoromethylamines. Organic Letters. 5: 2655-7. PMID 12868882 DOI: 10.1021/Ol034812M |
0.437 |
|
| 2003 |
Quiclet-Sire B, Sanchez-Jimenez G, Zard SZ. A new, unexpected synthesis of 1,3-dithietanones. Chemical Communications (Cambridge, England). 1408-9. PMID 12841265 DOI: 10.1039/B302434B |
0.413 |
|
| 2003 |
Ouvry G, Zard SZ. Convergent access to ketones, vinyl esters and vinyl bromides by a tin-free radical addition-intramolecular hydrogen atom transfer. Chemical Communications (Cambridge, England). 778-9. PMID 12703819 DOI: 10.1039/B212841A |
0.45 |
|
| 2003 |
Bath S, Laso NM, Lopez-Ruiz H, Quiclet-Sire B, Zard SZ. A practical access to acyl radicals from acyl hydrazides. Chemical Communications (Cambridge, England). 204-5. PMID 12585392 DOI: 10.1039/B210764C |
0.458 |
|
| 2003 |
Bacqué E, Pautrat F, Zard SZ. A concise synthesis of the tricyclic skeleton of pleuromutilin and a new approach to cycloheptenes. Organic Letters. 5: 325-8. PMID 12556183 DOI: 10.1021/Ol027312M |
0.484 |
|
| 2003 |
Ouvry G, Zard SZ. New radical homoallylation reactions Synlett. 1627-1630. DOI: 10.1055/S-2003-41011 |
0.501 |
|
| 2003 |
Binot G, Quiclet-Sire B, Saleh T, Zard SZ. A convergent construction of quaternary centres and polycyclic structures Synlett. 382-386. DOI: 10.1055/S-2003-37110 |
0.351 |
|
| 2003 |
Gagosz F, Zard SZ. A practical radical based access to functionalised geminal bisphosphonates Synlett. 387-389. DOI: 10.1055/S-2003-37108 |
0.488 |
|
| 2003 |
Quiclet-Sire B, Quintero L, Sanchez-Jimenez G, Zard SZ. A practical variation on the Paal-Knorr pyrrole synthesis Synlett. 75-78. DOI: 10.1055/S-2003-36223 |
0.486 |
|
| 2003 |
Binot G, Zard SZ. Intermolecular additions of cyclobutanone derived radicals. A convergent, highly efficient access to polycyclic cyclobutane containing structures Tetrahedron Letters. 44: 7703-7706. DOI: 10.1016/J.Tetlet.2003.09.042 |
0.556 |
|
| 2003 |
Destarac M, Taton D, Zard SZ, Saleh T, Six Y. On the importance of xanthate substituents in the MADIX process Acs Symposium Series. 854: 536-550. |
0.637 |
|
| 2002 |
Cassayre J, Gagosz F, Zard SZ. A short synthesis of (+/-)-13-deoxyserratine. Angewandte Chemie (International Ed. in English). 41: 1783-5. PMID 19750716 DOI: 10.1002/1521-3773(20020517)41:10<1783::Aid-Anie1783>3.0.Co;2-I |
0.483 |
|
| 2002 |
Gagosz F, Zard SZ. Tin-free radical sequences under acidic conditions. Convergent access to azole-containing structures. Organic Letters. 4: 4345-8. PMID 12443094 DOI: 10.1021/Ol0270024 |
0.487 |
|
| 2002 |
Bacqué E, Pautrat F, Zard SZ. A flexible strategy for the divergent modification of pleuromutilin. Chemical Communications (Cambridge, England). 2312-3. PMID 12430417 DOI: 10.1039/B206568A |
0.383 |
|
| 2002 |
Quiclet-Sire B, Zard SZ. An expedient synthesis of homophthalimides. Chemical Communications (Cambridge, England). 2306-7. PMID 12430414 DOI: 10.1039/B207649G |
0.491 |
|
| 2002 |
Quiclet-Sire B, Wendeborn F, Zard SZ. A new synthesis of pyrroles. Chemical Communications (Cambridge, England). 2214-5. PMID 12397984 DOI: 10.1039/B207061H |
0.454 |
|
| 2002 |
Quiclet-Sire B, Sortais B, Zard SZ. A convergent approach to 3-substituted-5-methoxyindoles. Application to the synthesis of melatonin [correction]. Chemical Communications (Cambridge, England). 1692-3. PMID 12196953 DOI: 10.1039/B204371H |
0.435 |
|
| 2002 |
Lusinchi M, Stanbury TV, Zard SZ. A convergent, flexible synthesis of 1,3-dienes. Chemical Communications (Cambridge, England). 1532-3. PMID 12189879 DOI: 10.1039/B203975C |
0.487 |
|
| 2002 |
Gagosz F, Moutrille C, Zard SZ. A new tin-free source of amidyl radicals. Organic Letters. 4: 2707-9. PMID 12153215 DOI: 10.1021/Ol026221M |
0.475 |
|
| 2002 |
Miranda LD, Zard SZ. A Short Synthesis of the Erythrina Skeleton and of (±)-α-Lycorane Organic Letters. 4: 1135-1138. PMID 11922801 DOI: 10.1021/Ol025534E |
0.718 |
|
| 2002 |
Renard D, Rezaei H, Zard SZ. A new convergent approach to α-branched alkynes Synlett. 1257-1260. DOI: 10.1055/S-2002-32956 |
0.457 |
|
| 2002 |
Quiclet-Sire B, Sortais B, Zard SZ. A convergent and flexible approach to hydroxylamines, hydrazines and related structures Synlett. 903-906. DOI: 10.1055/S-2002-31899 |
0.458 |
|
| 2002 |
Barbier F, Pautrat F, Quiclet-Sire B, Zard SZ. A mild exchange reaction of xanthates with bromine Synlett. 811-813. DOI: 10.1055/S-2002-25343 |
0.393 |
|
| 2002 |
Kalaï C, Tate E, Zard SZ. A short formal route to (±)-lepadin B using a xanthate-mediated free radical cyclisation/vinylation sequence Chemical Communications. 1430-1431. DOI: 10.1039/B203604E |
0.562 |
|
| 2002 |
Tate EW, Zard SZ. Efficient construction of polycyclic alkaloid synthetic precursors by a xanthate free radical addition and Mannich cyclisation cascade Tetrahedron Letters. 43: 4683-4686. DOI: 10.1016/S0040-4039(02)00835-3 |
0.681 |
|
| 2002 |
Dublanchet AC, Lusinchi M, Zard SZ. Xanthates and solid-phase chemistry. A new soluble polymer analogue of Wang resin Tetrahedron. 58: 5715-5721. DOI: 10.1016/S0040-4020(02)00526-4 |
0.369 |
|
| 2002 |
Quiclet-Sire B, Zard SZ, Zhang H. A practical access to α-phosphonoenamides Journal of Organometalic Chemistry. 643: 404-408. DOI: 10.1016/S0022-328X(01)01254-2 |
0.366 |
|
| 2002 |
Destarac M, Bzducha W, Taton D, Gauthier-Gillaizeau I, Zard SZ. Xanthates as chain-transfer agents in controlled radical polymerization (MADIX): Structural effect of the O-alkyl group Macromolecular Rapid Communications. 23: 1049-1054. DOI: 10.1002/Marc.200290002 |
0.343 |
|
| 2002 |
Destarac M, Brochon C, Catala JM, Wilczewska A, Zard SZ. Macromolecular Design via the Interchange of Xanthates (MADIX): Polymerization of styrene with O-ethyl xanthates as controlling agents Macromolecular Chemistry and Physics. 203: 2281-2289. DOI: 10.1002/Macp.200290002 |
0.319 |
|
| 2001 |
Huppé S, Rezaei H, Zard SZ. A new synthesis of 1-chloroalkynes. Chemical Communications (Cambridge, England). 1894-5. PMID 12240367 DOI: 10.1039/B106657A |
0.345 |
|
| 2001 |
Kaoudi T, Miranda LD, Zard SZ. An easy entry into berbane and alloyohimbane alkaloids via a 6-exo radical cyclization Organic Letters. 3: 3125-3127. PMID 11574011 DOI: 10.1021/Ol016424V |
0.508 |
|
| 2001 |
Lopez-Ruiz H, Zard SZ. A flexible access to highly functionalised boronates Chemical Communications. 2618-2619. DOI: 10.1039/B109637K |
0.499 |
|
| 2001 |
Boutillier P, Zard SZ. Synthetic equivalents of alkynyl and propargyl radicals Chemical Communications. 1304-1305. DOI: 10.1039/B101751I |
0.469 |
|
| 2001 |
Bertrand F, Pevere V, Quiclet-Sire B, Zard SZ. A xanthate transfer radical process for the introduction of the Trifluoromethyl group Organic Letters. 3: 1069-1071. DOI: 10.1021/Ol0156446 |
0.423 |
|
| 2001 |
Bertrand F, Le Guyader F, Liguori L, Ouvry G, Quiclet-Sire B, Seguin S, Zard SZ. α-Scission of sulfonyl radicals: A versatile process for organic synthesis Comptes Rendus De L'Academie Des Sciences - Series Iic: Chemistry. 4: 547-555. DOI: 10.1016/S1387-1609(01)01270-1 |
0.494 |
|
| 2001 |
Cassayre J, Zard SZ. A short synthesis of (-)-dendrobine. Some observations on the nickel mediated radical cyclisation and on the Pauson-Khand reaction Journal of Organometallic Chemistry. 624: 316-326. DOI: 10.1016/S0022-328X(01)00662-3 |
0.501 |
|
| 2000 |
Cassayre J, Dauge D, Zard SZ. Influence of copper(II) acetate on Ni/AcOH-promoted 5-endo and 5-exo radical cyclisations of trichloroacetamides Synlett. 471-474. DOI: 10.1055/S-2000-6556 |
0.368 |
|
| 2000 |
Cholleton N, Gauthier-Gillaizeau I, Six Y, Zard SZ. A new approach to cyclohexenes and related structures Chemical Communications. 535-536. DOI: 10.1039/B001119N |
0.753 |
|
| 2000 |
Legrand N, Quiclet-Sire B, Zard SZ. Radical addition to strained olefins: A flexible access to small ring derivatives Tetrahedron Letters. 41: 9815-9818. DOI: 10.1016/S0040-4039(00)01777-9 |
0.406 |
|
| 2000 |
Quiclet-Sire B, Wilczewska A, Zard SZ. A practical process for polymer-supported synthesis Tetrahedron Letters. 41: 5673-5677. DOI: 10.1016/S0040-4039(00)00886-8 |
0.334 |
|
| 2000 |
Destarac M, Charmot D, Franck X, Zard SZ. Dithiocarbamates as universal reversible addition-fragmentation chain transfer agents Macromolecular Rapid Communications. 21: 1035-1039. DOI: 10.1002/1521-3927(20001001)21:15<1035::Aid-Marc1035>3.0.Co;2-5 |
0.371 |
|
| 2000 |
Kaoudi T, Quiclet-Sire B, Seguin S, Zard SZ. An expedient construction of seven-membered rings adjoining aromatic systems Angewandte Chemie - International Edition. 39: 731-733. DOI: 10.1002/(Sici)1521-3773(20000218)39:4<731::Aid-Anie731>3.0.Co;2-U |
0.44 |
|
| 1999 |
Bertrand F, Quiclet-Sire B, Zard SZ. A New Radical Vinylation Reaction of Iodides and Dithiocarbonates. Angewandte Chemie (International Ed. in English). 38: 1943-1946. PMID 34182663 DOI: 10.1002/(SICI)1521-3773(19990712)38:13/14<1943::AID-ANIE1943>3.0.CO;2-R |
0.367 |
|
| 1999 |
Quiclet-Sire B, Zard SZ. Some new radical reactions for organic synthesis Phosphorus, Sulfur and Silicon and Related Elements. 153: 137-154. DOI: 10.1080/10426509908546431 |
0.493 |
|
| 1999 |
Gagosz F, Zard SZ. Generation and capture of iminyl radicals from ketoxime xanthates Synlett. 1978-1980. DOI: 10.1055/S-1999-2971 |
0.39 |
|
| 1999 |
Cassayre J, Zard SZ. A short synthesis of γ-lycorane using Ni/AcOH mediated radical cyclisation Synlett. 501-503. DOI: 10.1055/S-1999-2621 |
0.414 |
|
| 1999 |
Cassayre J, Zard SZ. A Short Synthesis of (−)-Dendrobine Journal of the American Chemical Society. 121: 6072-6073. DOI: 10.1021/Ja990707P |
0.314 |
|
| 1999 |
Boivin J, Pothier J, Ramos L, Zard SZ. An expeditious construction of 9-membered rings Tetrahedron Letters. 40: 9239-9241. DOI: 10.1016/S0040-4039(99)01965-6 |
0.795 |
|
| 1999 |
Boivin J, Pothier J, Zard SZ. A flexible, convergent approach to piperidines, pyridines, azepines, and related derivatives Tetrahedron Letters. 40: 3701-3704. DOI: 10.1016/S0040-4039(99)00592-4 |
0.818 |
|
| 1999 |
Ly TM, Quiclet-Sire B, Sortais B, Zard SZ. A convergent approach to indolines and indanes Tetrahedron Letters. 40: 2533-2536. DOI: 10.1016/S0040-4039(99)00286-5 |
0.49 |
|
| 1999 |
Boivin J, Boutillier P, Zard SZ. An unusual and highly efficient access to thieno[2,3-b]-benzothiopyran structures Tetrahedron Letters. 40: 2529-2532. DOI: 10.1016/S0040-4039(99)00285-3 |
0.361 |
|
| 1999 |
Hoang-Cong X, Quiclet-Sire B, Zard SZ. An expedient synthesis of (±)-γ-lycorane Tetrahedron Letters. 40: 2125-2126. DOI: 10.1016/S0040-4039(99)00146-X |
0.364 |
|
| 1999 |
Fauré-Tromeur M, Zard SZ. Preparation of olefins from alcohols by thermal rearrangement of propargylic xanthates Tetrahedron Letters. 40: 1305-1308. DOI: 10.1016/S0040-4039(98)02669-0 |
0.307 |
|
| 1999 |
Bouhadir G, Legrand N, Quiclet-Sire B, Zard SZ. A new practical synthesis of tertiary S-alkyl dithiocarbonates and related derivatives Tetrahedron Letters. 40: 277-280. DOI: 10.1016/S0040-4039(98)02380-6 |
0.442 |
|
| 1999 |
Forbes JE, Saicic RN, Zard SZ. New radical reactions of S-alkoxycarbonyl xanthates. Total synthesis of (±)-cinnamolide and (±)-methylenolactocin Tetrahedron. 55: 3791-3802. DOI: 10.1016/S0040-4020(98)01184-3 |
0.389 |
|
| 1999 |
Quiclet-Sire B, Zard SZ. Some new radical reactions of xanthates Journal of the Chinese Chemical Society. 46: 139-145. DOI: 10.1002/Jccs.199900021 |
0.48 |
|
| 1999 |
Bertrand F, Quiclet-Sire B, Zard SZ. A new radical vinylation reaction of iodides and dithiocarbonates Angewandte Chemie - International Edition. 38: 1943-1946. DOI: 10.1002/(Sici)1521-3773(19990712)38:13/14<1943::Aid-Anie1943>3.0.Co;2-R |
0.471 |
|
| 1998 |
Quiclet-Sire B, Seguin S, Zard SZ. A New Radical Allylation Reaction of Dithiocarbonates. Angewandte Chemie (International Ed. in English). 37: 2864-2866. PMID 29711112 DOI: 10.1002/(SICI)1521-3773(19981102)37:20<2864::AID-ANIE2864>3.0.CO;2-W |
0.397 |
|
| 1998 |
Boiteau L, Boivin J, Liard A, Quiclet-Sire B, Zard SZ. A Short Synthesis of (±)-Matrine. Angewandte Chemie (International Ed. in English). 37: 1128-1131. PMID 29711036 DOI: 10.1002/(Sici)1521-3773(19980504)37:8<1128::Aid-Anie1128>3.0.Co;2-P |
0.449 |
|
| 1998 |
Quiclet-Sire B, Zard SZ. A practical modification of the Barton-McCombie reaction and radical O- to S- rearrangement of xanthates Tetrahedron Letters. 39: 9435-9438. DOI: 10.1016/S0040-4039(98)02187-X |
0.372 |
|
| 1998 |
Cassayre J, Quiclet-Sire B, Saunier JB, Zard SZ. Nickel powder promoted 5-endo radical cyclisations. A concise approach to erythrina alkaloids Tetrahedron Letters. 39: 8995-8998. DOI: 10.1016/S0040-4039(98)02036-X |
0.478 |
|
| 1998 |
Fauré-Tromeur M, Zard SZ. A practical synthesis of benzyl esters and related derivatives Tetrahedron Letters. 39: 7301-7304. DOI: 10.1016/S0040-4039(98)01563-9 |
0.41 |
|
| 1998 |
Cholleton N, Zard SZ. A convergent synthesis of 4-substituted 1,2,3,4 tetrahydroisoquinolin- 1-ones Tetrahedron Letters. 39: 7295-7298. DOI: 10.1016/S0040-4039(98)01561-5 |
0.496 |
|
| 1998 |
Boivin J, Ramos L, Zard SZ. An expedient radical based approach to difluorophosphonate analogues of thionucleosides Tetrahedron Letters. 39: 6877-6880. DOI: 10.1016/S0040-4039(98)01501-9 |
0.479 |
|
| 1998 |
Quiclet-Sire B, Zard SZ. A concise access to a new class of selective anti-inflammatory steroid derivatives Tetrahedron Letters. 39: 1173-1174. DOI: 10.1016/S0040-4039(97)10809-7 |
0.334 |
|
| 1998 |
Biadatti T, Quiclet-Sire B, Saunier J, Zard SZ. The Tetrazolylmethyl and Related Radicals: A Convenient Access to Tetrazoles and Other Heterocyclic Derivatives Tetrahedron Letters. 39: 19-22. DOI: 10.1016/S0040-4039(97)10457-9 |
0.391 |
|
| 1998 |
Barton DHR, Géro SD, Holliday P, Quiclet-Sire B, Zard SZ. A practical decarboxylative hydroxylation of carboxylic acids Tetrahedron. 54: 6751-6756. DOI: 10.1016/S0040-4020(98)00337-8 |
0.328 |
|
| 1998 |
Ly TM, Laso NM, Zard SZ. A new synthesis of 3-aryl substituted oxindoles Tetrahedron. 54: 4889-4898. DOI: 10.1016/S0040-4020(98)00172-0 |
0.47 |
|
| 1998 |
Boiteau L, Boivin J, Quiclet-Sire B, Saunier J, Zard SZ. Synthetic routes to β-lactams. Some unexpected hydrogen atom transfer reactions Tetrahedron. 54: 2087-2098. DOI: 10.1016/S0040-4020(97)10417-3 |
0.414 |
|
| 1998 |
Cassayre J, Quiclet-Sire B, Saunier J, Zard SZ. β- and γ-lactams by nickel powder mediated 4-exo or 5-endo radical cyclisations. A concise construction of the mesembrine skeleton Tetrahedron. 54: 1029-1040. DOI: 10.1016/S0040-4020(97)10204-6 |
0.49 |
|
| 1998 |
Sire B, Seguin S, Zard SZ. A new radical allylation reaction of dithiocarbonates Angewandte Chemie - International Edition. 37: 2864-2866. DOI: 10.1002/(SICI)1521-3773(19981102)37:20<2864::AID-ANIE2864>3.0.CO;2-W |
0.335 |
|
| 1997 |
Quiclet-Sire B, Zard SZ. Riding The Tiger : Using Degeneracy To Tame Wild Radical Processes Pure and Applied Chemistry. 69: 645-650. DOI: 10.1351/Pac199769030645 |
0.466 |
|
| 1997 |
Boivin J, Quiclet-Sire B, Ramos L, Zard SZ. New reductive deiodination reaction by hydrogen atom transfer from cyclohexane Chemical Communications. 353-354. DOI: 10.1039/A607459F |
0.368 |
|
| 1997 |
Le Guyader F, Quiclet-Sire B, Seguin S, Zard SZ. New radical allylation reaction of iodides Journal of the American Chemical Society. 119: 7410-7411. DOI: 10.1021/Ja9708878 |
0.449 |
|
| 1997 |
Boivin J, Yousfi M, Zard SZ. Spirolactams by a novel ipso-radical cyclisation and loss of aromaticity Tetrahedron Letters. 38: 5985-5988. DOI: 10.1016/S0040-4039(97)01362-2 |
0.455 |
|
| 1997 |
Callier-Dublanchet A, Quiclet-Sire B, Zard* SZ. Iminyl Radical Generation via Iminodithiocarbonate Group Transfer Tetrahedron Letters. 38: 2463-2466. DOI: 10.1016/S0040-4039(97)00384-5 |
0.418 |
|
| 1997 |
Liard A, Quiclet-Sire B, Saicic RN, Zard SZ. A new synthesis of α-tetralones Tetrahedron Letters. 38: 1759-1762. DOI: 10.1016/S0040-4039(97)00184-6 |
0.349 |
|
| 1997 |
Zard SZ. On the Trail of Xanthates: Some New Chemistry from an Old Functional Group Angewandte Chemie International Edition in English. 36: 672-685. DOI: 10.1002/Anie.199706721 |
0.505 |
|
| 1996 |
Zard SZ. Iminyl Radicals: A Fresh Look at a Forgotten Species (and Some of its Relatives) Synlett. 1996: 1148-1154. DOI: 10.1055/S-1996-5698 |
0.312 |
|
| 1996 |
Denieul M, Quiclet-Sire B, Zard SZ. Trifluoroacetonyl radicals: a versatile approach to trifluoromethyl ketones Chemical Communications. 2511-2512. DOI: 10.1039/Cc9960002511 |
0.463 |
|
| 1996 |
Saicic RN, Zard SZ. Total synthesis of (±)-cinnamolide and (±)-methylenolactocin–an approach to butenolides using S-alkoxycarbonyl xanthates Chemical Communications. 1631-1632. DOI: 10.1039/Cc9960001631 |
0.317 |
|
| 1996 |
Poelert M, Roger W, Zard SZ. A new carbon–carbon bond forming reaction using O-methyl (S)-prop-2-ynyl dithiocarbonate Chemical Communications. 743-744. DOI: 10.1039/Cc9960000743 |
0.356 |
|
| 1996 |
Quiclet-Sire B, Zard SZ. An Unusual Route to Deoxysugars by Hydrogen Atom Transfer from Cyclohexane. Possible Manifestation of Polar Effects in a Radical Process Journal of the American Chemical Society. 118: 9190-9191. DOI: 10.1021/Ja9619622 |
0.313 |
|
| 1996 |
Quiclet-Sire B, Zard SZ. New Radical Allylation Reaction Journal of the American Chemical Society. 118: 1209-1210. DOI: 10.1021/Ja9522443 |
0.444 |
|
| 1996 |
Quiclet-Sire B, Saicic RN, Zard SZ. A convenient synthesis of trifluoromethyl aryl sulfides Tetrahedron Letters. 37: 9057-9058. DOI: 10.1016/S0040-4039(96)02127-2 |
0.401 |
|
| 1996 |
Boivin J, Huppé S, Zard SZ. A convergent approach to functionalised alkynes Tetrahedron Letters. 37: 8735-8738. DOI: 10.1016/S0040-4039(96)02015-1 |
0.414 |
|
| 1996 |
Denieul M, Quiclet-Sire B, Zard SZ. A synthetically useful source of propargyl radicals Tetrahedron Letters. 37: 5495-5498. DOI: 10.1016/0040-4039(96)01146-X |
0.372 |
|
| 1996 |
Laso NM, Quiclet-Sire B, Zard SZ. A new selective reduction of nitroalkenes into enamides Tetrahedron Letters. 37: 1605-1608. DOI: 10.1016/0040-4039(96)00078-0 |
0.305 |
|
| 1996 |
Quiclet-Sire B, Saunier J, Zard SZ. β-Lactams by a nickel powder/acetic acid mediated radical cyclisation Tetrahedron Letters. 37: 1397-1400. DOI: 10.1016/0040-4039(96)00033-0 |
0.402 |
|
| 1995 |
Poelert MA, Zard SZ. A New Reaction of S-Propargyl Dithiocarbonates (Xanthates) with Acid Chlorides Synlett. 1995: 325-326. DOI: 10.1055/S-1995-4957 |
0.369 |
|
| 1995 |
Quiclet-Sire B, Thévenot I, Zard SZ. A new and practical synthesis of pyrroles Tetrahedron Letters. 36: 9469-9470. DOI: 10.1016/0040-4039(95)02001-2 |
0.39 |
|
| 1995 |
Callier-Dublanchet A, Quiclet-Sire B, Zard SZ. A new source of nitrogen centered radicals Tetrahedron Letters. 36: 8791-8794. DOI: 10.1016/0040-4039(95)01878-L |
0.422 |
|
| 1995 |
Boivin J, Lallemand JY, Schmitt A, Zard SZ. Reduction of activated thiopyridyl compounds by zinc metal Tetrahedron Letters. 36: 7243-7246. DOI: 10.1016/0040-4039(95)01497-6 |
0.347 |
|
| 1995 |
Boivin J, Huppé S, Zard SZ. An efficient synthesis of large ring acetylenes Tetrahedron Letters. 36: 5737-5740. DOI: 10.1016/0040-4039(95)01146-9 |
0.421 |
|
| 1995 |
Boivin J, Henriet EB, Zard SZ. A new access to 1,3-dithiol-2-ylidenes from S-propargyl dithiocarbonates (xanthates) Tetrahedron Letters. 36: 5171-5174. DOI: 10.1016/0040-4039(95)00939-A |
0.316 |
|
| 1995 |
Boivin J, Pillot E, Williams A, Roger W, Zard SZ. On the mechanism of the nitrous acid induced conversion of an isopropylidene group into an alkyne Tetrahedron Letters. 36: 3333-3336. DOI: 10.1016/0040-4039(95)00522-E |
0.401 |
|
| 1995 |
Boivin J, Callier-Dublanchet A, Quiclet-Sire B, Schiano A, Zard SZ. Iminyl, amidyl, and carbamyl radicals from O-benzoyl oximes and O-benzoyl hydroxamic acid derivatives Tetrahedron. 51: 6517-6528. DOI: 10.1016/0040-4020(95)00319-4 |
0.363 |
|
| 1995 |
Boivin J, El Kaim L, Zard SZ. Trifluoromethyl ketones from carboxylic acids. Part II. A versatile access to trifluoromethylated heterocycles Tetrahedron. 51: 2585-2592. DOI: 10.1016/0040-4020(95)00007-U |
0.444 |
|
| 1995 |
Boivin J, Kaim LE, Zard SZ. A new and efficient synthesis of trifluoromethyl ketones from carboxylic acids. Part I Tetrahedron. 51: 2573-2584. DOI: 10.1016/0040-4020(95)00006-T |
0.789 |
|
| 1995 |
Barlaam B, Boivin J, Elkaim L, Elton-Farr S, Zard SZ. A short total synthesis of estrone derivatives: A novel 1,3-rearrangement of an allylic nitro group Tetrahedron. 51: 1675-1684. DOI: 10.1016/0040-4020(94)01034-W |
0.392 |
|
| 1994 |
Boivin J, Henriet E, Zard SZ. A Highly Efficient Reaction for the Synthesis of Esters and for the Inversion of Secondary Alcohols Journal of the American Chemical Society. 116: 9739-9740. DOI: 10.1021/Ja00100A045 |
0.369 |
|
| 1994 |
Boivin J, Yousfi M, Zard SZ. A versatile radical based synthesis of γ-lactams using nickel powder / acetic acid Tetrahedron Letters. 35: 5629-5632. DOI: 10.1016/S0040-4039(00)77265-0 |
0.466 |
|
| 1994 |
Boivin J, Schiano AM, Zard SZ. Iminyl radicals by stannane mediated cleavage of oxime esters Tetrahedron Letters. 35: 249-252. DOI: 10.1016/S0040-4039(00)76523-3 |
0.475 |
|
| 1994 |
Boivin J, Fouquet E, Schiano A, Zard SZ. Iminyl radicals: Part III. Further synthetically useful sources of iminyl radicals. Tetrahedron. 50: 1769-1776. DOI: 10.1016/S0040-4020(01)80851-6 |
0.439 |
|
| 1994 |
Boivin J, Fouquet E, Zard SZ. Iminyl radicals: part II. ring opening of cyclobutyl- and cyclopentyliminyl radicals Tetrahedron. 50: 1757-1768. DOI: 10.1016/S0040-4020(01)80850-4 |
0.47 |
|
| 1994 |
Boivin J, Fouquet E, Zard SZ. Iminyl radicals: Part I. generation and intramolecular capture by an olefin Tetrahedron. 50: 1745-1756. DOI: 10.1016/S0040-4020(01)80849-8 |
0.494 |
|
| 1994 |
Boivin J, Yousfi M, Zard SZ. A new and practical synthesis of indolones Tetrahedron Letters. 35: 9553-9556. DOI: 10.1016/0040-4039(94)88509-5 |
0.461 |
|
| 1994 |
Axon J, Boiteau L, Boivin J, Forbes JE, Zard SZ. A new radical based synthesis of lactams and indolones from dithiocarbonates (xanthates) Tetrahedron Letters. 35: 1719-1722. DOI: 10.1016/0040-4039(94)88328-9 |
0.481 |
|
| 1994 |
Callier A, Quiclet-Sire B, Zard SZ. Amidyl and carbamyl radicals by stannane mediated cleavage of O-benzoyl hydroxamic acid derivatives Tetrahedron Letters. 35: 6109-6112. DOI: 10.1016/0040-4039(94)88089-1 |
0.39 |
|
| 1993 |
Barlaam B, Boivin J, Zard SZ. A new synthesis of substituted dienes by reductive elimination of allylic nitro derivatives Tetrahedron Letters. 34: 1023-1026. DOI: 10.1016/S0040-4039(00)77482-X |
0.44 |
|
| 1993 |
Forbes J, Zard SZ. Xanthic anhydrides: A novel and convenient source of alkoxythiocarbonyl and alkyl radicals. Tetrahedron. 49: 8257-8266. DOI: 10.1016/S0040-4020(01)88043-1 |
0.452 |
|
| 1993 |
Barton DH, Gateau-Olesker A, Géro SD, Lacher B, Tachdjian C, Zard SZ. Radical decarboxylative alkylation of tartaric acid Tetrahedron. 49: 4589-4602. DOI: 10.1016/S0040-4020(01)81288-6 |
0.63 |
|
| 1992 |
Boivin J, Camara J, Zard SZ. Novel radical chain reactions based on O-alkyl tin dithiocarbonates Journal of the American Chemical Society. 114: 7909-7910. DOI: 10.1021/Ja00046A045 |
0.415 |
|
| 1992 |
Boivin J, Kaim LE, Zard SZ. An expedient access to trifluoromethyl ketones from carboxylic acids Tetrahedron Letters. 33: 1285-1288. DOI: 10.1016/S0040-4039(00)91602-2 |
0.784 |
|
| 1992 |
Boivin J, Tailhan C, Zard SZ. An unusual access to 4,5-bis(alkylidene)-1,3-dithiolan-2-ones: A new class of cisoid dienes Tetrahedron Letters. 33: 7853-7856. DOI: 10.1016/S0040-4039(00)74761-7 |
0.305 |
|
| 1992 |
Boivin J, Schiano AM, Zard SZ. A novel and practical access to 13-epi-17-ketosteroids Tetrahedron Letters. 33: 7849-7852. DOI: 10.1016/S0040-4039(00)74760-5 |
0.34 |
|
| 1992 |
Boivin J, Chauvet C, Zard SZ. A convenient access to 16-methylene and 16β-methyl corticosteroids by a novel transformation of geminal bis(phenylsulphinyl) intermediates Tetrahedron Letters. 33: 4913-4916. DOI: 10.1016/S0040-4039(00)61232-7 |
0.371 |
|
| 1991 |
Boivin J, Tailhan C, Zard SZ. Novel formal 3 + 2 annulation reaction based on S-propargyl dithiocarbonates (xanthates) Journal of the American Chemical Society. 113: 5874-5876. DOI: 10.1021/Ja00015A058 |
0.356 |
|
| 1991 |
Boivin J, Fouquet E, Zard SZ. Ring opening induced by iminyl radicals derived from cyclobutanones: new aspects of tin hydride cleavage of S-phenyl sulfenylimines Journal of the American Chemical Society. 113: 1055-1057. DOI: 10.1021/Ja00003A057 |
0.457 |
|
| 1991 |
Boivin J, Elkaim L, Ferro PG, Zard SZ. A new practical method for the synthesis of acetylenes. Tetrahedron Letters. 32: 5321-5324. DOI: 10.1016/S0040-4039(00)92375-X |
0.467 |
|
| 1991 |
Boivin J, Fouquet E, Zard SZ. A new and synthetically useful source of iminyl radicals Tetrahedron Letters. 32: 4299-4302. DOI: 10.1016/S0040-4039(00)92153-1 |
0.45 |
|
| 1991 |
Barlaam B, Boivin J, El Kaim L, Zard SZ. An expedient total synthesis of (±)-estrone derivatives Tetrahedron Letters. 32: 623-626. DOI: 10.1016/S0040-4039(00)74843-X |
0.32 |
|
| 1991 |
Newcomb M, Udaya Kumar M, Voivin J, Crépon (née daSilva) E, Zard SZ. Cyclizations and intermolecular additions of alkoxycarbonyloxy radicals from N-hydroxypyridine-2-thione carbonates Tetrahedron Letters. 32: 45-48. DOI: 10.1016/S0040-4039(00)71214-7 |
0.395 |
|
| 1991 |
Boivin J, Crépon (née da Silva) E, Zard SZ. Further observations on the thermal stability of N-hydroxy-2-thiopyridone esters: improved decarboxylative radical additions to olefins Tetrahedron Letters. 32: 199-202. DOI: 10.1016/0040-4039(91)80854-Y |
0.454 |
|
| 1990 |
Forbes JE, Zard SZ. New radical chain reaction of S-alkoxycarbonyl dithiocarbonates: a useful source of alkyl radicals from alcohols Journal of the American Chemical Society. 112: 2034-2036. DOI: 10.1021/Ja00161A078 |
0.411 |
|
| 1990 |
Boivin J, da Silva E, Ourisson G, Zard SZ. Proof of a radical transannular hydrogen migration in the longifolene series. Tetrahedron Letters. 31: 2501-2504. DOI: 10.1016/S0040-4039(00)97400-8 |
0.456 |
|
| 1990 |
Boivin J, Crépon (née da Silva) E, Zard SZ. N-hydroxy-2-pyridinethione: A mild and convenient source of hydroxyl radicals Tetrahedron Letters. 31: 6869-6872. DOI: 10.1016/S0040-4039(00)97193-4 |
0.413 |
|
| 1990 |
Boivin J, Fouquet E, Zard SZ. Multiple radical additions starting with iminyl radicals derived from sulphenylimines Tetrahedron Letters. 31: 3545-3548. DOI: 10.1016/S0040-4039(00)94438-1 |
0.471 |
|
| 1990 |
Boivin J, Fouquet E, Zard SZ. Cyclisation of imine radicals derived from sulphenylimines: A simple access to Δ1-pyrrolines Tetrahedron Letters. 31: 85-88. DOI: 10.1016/S0040-4039(00)94340-5 |
0.453 |
|
| 1990 |
Barlaam B, Boivin J, Zard SZ. A practical access to allylic sulphones and lactones from allylic nitro compounds Tetrahedron Letters. 31: 7429-7432. DOI: 10.1016/S0040-4039(00)88507-X |
0.445 |
|
| 1990 |
H.R. Barton D, Kervagoret J, Zard SZ. A useful synthesis of pyrroles from nitroolefins Tetrahedron. 46: 7587-7598. DOI: 10.1016/S0040-4020(01)89069-4 |
0.402 |
|
| 1990 |
BOIVIN J, FOUQUET E, ZARD SZ. ChemInform Abstract: Cyclization of Imine Radicals Derived from Sulfenylimines: A Simple Access to δ1-Pyrrolines. Cheminform. 21. DOI: 10.1002/chin.199037174 |
0.404 |
|
| 1990 |
FORBES JE, ZARD SZ. ChemInform Abstract: A Novel Radical Chain Reaction of Xanthic Anhydrides. Further Observations on the Intermediacy of Alkoxythiocarbonyl Radicals in the Barton-McCombie Reaction. Cheminform. 21. DOI: 10.1002/chin.199012116 |
0.338 |
|
| 1989 |
Boivin J, Kaim LE, Kervagoret J, Zard SZ. A novel thermal rearrangement of allylic nitro derivatives into allylic alcohols Journal of the Chemical Society, Chemical Communications. 1006-1008. DOI: 10.1039/C39890001006 |
0.312 |
|
| 1989 |
Barton DH, Boivin J, Sarma J, da Silva E, Zard SZ. Some further novel transformations of geminal (pyridine-2-thiyl) phenylsulphones Tetrahedron Letters. 30: 4237-4240. DOI: 10.1016/S0040-4039(01)80699-7 |
0.605 |
|
| 1989 |
Forbes J, Zard S. A novel radical chain reaction of xanthic anhydrides. Further observations on the intermediacy of alkoxy-thiocarbonyl radicals in the Barton-McCombie reaction Tetrahedron Letters. 30: 4367-4370. DOI: 10.1016/S0040-4039(00)99362-6 |
0.429 |
|
| 1989 |
Barton DH, Bridon D, Zard SZ. The invention of radical reactions. Part XVIII. Decarboxylative radical addition to arsenic, antimony, and bismuth phenylsulphides - a novel synthesis of nor-alcohols from carboxylic acids Tetrahedron. 45: 2615-2626. DOI: 10.1016/S0040-4020(01)80092-2 |
0.362 |
|
| 1989 |
BARTON DHR, WOZNIAK J, ZARD SZ. ChemInform Abstract: A Short and Efficient Degradation of the Bile Acid Side Chain. Some Novel Reactions of Sulfines and α-Keto Esters. Cheminform. 20. DOI: 10.1002/chin.198943253 |
0.332 |
|
| 1989 |
BARTON DHR, BRIDON D, ZARD SZ. ChemInform Abstract: The Invention of Radical Reactions. Part 18. Decarboxylative Radical Addition to Arsenic, Antimony, and Bismuth Phenylsulfides. A Novel Synthesis of Noralcohols from Carboxylic Acids. Cheminform. 20. DOI: 10.1002/chin.198935141 |
0.431 |
|
| 1988 |
Delduc P, Tailhan C, Zard SZ. A convenient source of alkyl and acyl radicals Journal of the Chemical Society, Chemical Communications. 308-310. DOI: 10.1039/C39880000308 |
0.437 |
|
| 1988 |
Barton DHR, Silva Ed, Zard SZ. Multiple radical additions: an expedient entry into complex frameworks Journal of the Chemical Society, Chemical Communications. 285-287. DOI: 10.1039/C39880000285 |
0.417 |
|
| 1988 |
Barton DH, Bowles T, Husinec S, Forbes JE, Llobera A, Porter AE, Zard SZ. Reductive formylation of oximes; an approach to the synthesis of vinyl isonitriles Tetrahedron Letters. 29: 3343-3346. DOI: 10.1016/0040-4039(88)85157-8 |
0.619 |
|
| 1988 |
DELDUC P, TAILHAN C, ZARD SZ. ChemInform Abstract: A Convenient Source of Alkyl and Acyl Radicals. Cheminform. 19. DOI: 10.1002/chin.198831075 |
0.319 |
|
| 1988 |
BARTON DHR, LACHER B, MISTERKIEWICZ B, ZARD SZ. ChemInform Abstract: The Invention of Radical Reactions. Part 17. A Decarboxylative Sulfonylation of Carboxylic Acids. Cheminform. 19. DOI: 10.1002/chin.198825109 |
0.359 |
|
| 1987 |
Barton DHR, Gateau-Olesker A, Gero SD, Lacher B, Tachdjian C, Zard SZ. Stereospecificity in radical carbon–carbon bond formation reactions based on tartaric acid Journal of the Chemical Society, Chemical Communications. 1790-1792. DOI: 10.1039/C39870001790 |
0.489 |
|
| 1987 |
Barton DHR, Wozniak J, Zard SZ. A very short degradation of the bile acid side chain Journal of the Chemical Society, Chemical Communications. 1383-1385. DOI: 10.1039/C39870001383 |
0.426 |
|
| 1987 |
H.R. Barton D, Lacher B, Zard SZ. The invention of radical reactions Tetrahedron. 43: 4321-4328. DOI: 10.1016/S0040-4020(01)90307-2 |
0.496 |
|
| 1987 |
Barton DH, Bridon D, Fernandaz-Picot I, Zard SZ. The invention of radical reactions Tetrahedron. 43: 2733-2740. DOI: 10.1016/S0040-4020(01)86878-2 |
0.312 |
|
| 1987 |
BARTON DHR, BRIDON D, ZARD SZ. ChemInform Abstract: The Invention of New Radical Chain Reactions. Part 13. High Yielding Decarboxylative Chalcogenation of Aliphatic and Alicyclic Acids. Cheminform. 18. DOI: 10.1002/chin.198726236 |
0.363 |
|
| 1986 |
Barton DHR, Motherwell WB, Simon ES, Zard SZ. Reduction of oximes and aliphatic nitro compounds to imines for further in situ reactions: a novel synthesis of pyrroles and pyrrolin-2-ones Journal of the Chemical Society-Perkin Transactions 1. 2243-2252. DOI: 10.1039/P19860002243 |
0.624 |
|
| 1986 |
Barton DH, Bridon D, Zard SZ. Radical decarboxylative phosphorylation of carboxylic acids Tetrahedron Letters. 27: 4309-4312. DOI: 10.1016/S0040-4039(00)94261-8 |
0.571 |
|
| 1986 |
Castagnino E, Corsano S, Barton DH, Zard SZ. Decarboxylative radical addition onto protonated heteroaromatic systems including purine bases Tetrahedron Letters. 27: 6337-6338. DOI: 10.1016/S0040-4039(00)87802-8 |
0.532 |
|
| 1986 |
Barton DH, Garcia B, Togo H, Zard SZ. Radical decarboxylative addition onto protonated heteroaromatic (and related) compounds Tetrahedron Letters. 27: 1327-1330. DOI: 10.1016/S0040-4039(00)84250-1 |
0.541 |
|
| 1986 |
Barton DH, Crich D, Löbberding A, Zard SZ. On the mechanism of the deoxygenation of secondary alcohols by the reduction of their methyl xanthates by tin hydrides Tetrahedron. 42: 2329-2338. DOI: 10.1016/S0040-4020(01)90614-3 |
0.483 |
|
| 1986 |
Barton DH, Lacher B, Zard SZ. The invention of new radical chain reactions Tetrahedron. 42: 2325-2328. DOI: 10.1016/S0040-4020(01)90613-1 |
0.302 |
|
| 1986 |
Barton DH, Bridon D, Hervé Y, Potier P, Thierry J, Zard SZ. Concise syntheses of L-selenomethionine and of L-selenocystine using radical chain reactions Tetrahedron. 42: 4983-4990. DOI: 10.1016/S0040-4020(01)88049-2 |
0.301 |
|
| 1986 |
BARTON DHR, TOGO H, ZARD SZ. ChemInform Abstract: Radical Addition to Vinyl Sulphones and Vinyl Phosphonium Salts. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198625114 |
0.369 |
|
| 1986 |
BARTON DHR, LACHER B, ZARD SZ. ChemInform Abstract: Radical Decarboxylative Bromination of Aromatic Acids. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198616140 |
0.341 |
|
| 1986 |
BARTON DHR, TOGO H, ZARD SZ. ChemInform Abstract: The Invention of New Radical Chain Reactions. Part 10. High Yield Radical Addition Reactions of αβ-Unsaturated Nitroolefins. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198613118 |
0.468 |
|
| 1985 |
Barton DHR, Zard SZ. A further synthesis of the corticosteroid side chain starting with a suitable 17-ketone Journal of the Chemical Society-Perkin Transactions 1. 17: 2191-2192. DOI: 10.1039/P19850002191 |
0.415 |
|
| 1985 |
Barton DHR, Motherwell WB, Wozniak J, Zard SZ. An efficient and short degradation of the cholic acid side chain: a new method for the preparation and dehydrogenation of 4,5-dihydro-oxazoles Journal of the Chemical Society-Perkin Transactions 1. 16: 1865-1869. DOI: 10.1039/P19850001865 |
0.603 |
|
| 1985 |
Barton DHR, Zard SZ. A new synthesis of pyrroles from nitroalkenes Journal of the Chemical Society, Chemical Communications. 1098-1100. DOI: 10.1039/C39850001098 |
0.415 |
|
| 1985 |
Barton DHR, Bridon D, Zard SZ. A convenient high yielding synthesis of nor-alcohols from carboxylic acids Journal of the Chemical Society, Chemical Communications. 1066-1068. DOI: 10.1039/C39850001066 |
0.334 |
|
| 1985 |
Barton DHR, Crich D, Löbberding A, Zard SZ. On the mechanism of reduction of dithiocarbonates (xanthates) with tributylstannane Journal of the Chemical Society, Chemical Communications. 646-647. DOI: 10.1039/C39850000646 |
0.534 |
|
| 1985 |
Barton DH, Togo H, Zard SZ. Radical addition to vinyl sulphones and vinyl phosphonium salts Tetrahedron Letters. 26: 6349-6352. DOI: 10.1016/S0040-4039(01)84596-2 |
0.607 |
|
| 1985 |
Barton DH, Lacher B, Zard SZ. Radical decarboxylative bromination of aromatic acids Tetrahedron Letters. 26: 5939-5942. DOI: 10.1016/S0040-4039(00)98266-2 |
0.587 |
|
| 1985 |
BARTON DHR, BRIDON D, ZARD SZ. ChemInform Abstract: A CONVENIENT HIGH YIELDING SYNTHESIS OF NORALCOHOLS FROM CARBOXYLIC ACIDS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198550098 |
0.404 |
|
| 1984 |
Barton DHR, Motherwell WB, Simon ES, Zard SZ. A mild and efficient method for the reduction of oximes to imines for futher in situ reactions Journal of the Chemical Society, Chemical Communications. 337-338. DOI: 10.1039/C39840000337 |
0.592 |
|
| 1984 |
Barton DH, Bridon D, Zard SZ. New decarboxylative chalcogenation of aliphatic and alicyclic carboxylic acids. Tetrahedron Letters. 25: 5777-5780. DOI: 10.1016/S0040-4039(01)81684-1 |
0.502 |
|
| 1984 |
Barton DHR, Motherwell WB, Zard SZ. A mild reduction of aliphatic nitro compounds to imines for further in situ reactions : A simple synthesis of pyrroles Tetrahedron Letters. 25: 3707-3710. DOI: 10.1016/0040-4039(84)80111-2 |
0.618 |
|
| 1984 |
Barton DHR, Motherwell WB, Simon ES, Zard SZ. A mild and efficient method for the reduction of oximes to imines for further in situ reactions Journal of the Chemical Society, Chemical Communications. 337-338. DOI: 10.1002/Chin.198429306 |
0.578 |
|
| 1983 |
BARTON DHR, MOTHERWELL WB, ZARD SZ. ChemInform Abstract: A SIMPLE AND ECONOMIC SYNTHESIS OF THE CORTICOSTEROID SIDE CHAIN FROM 17-OXO STEROIDS. IMPROVED KETONE-NITROMETHANE REACTIONS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198343312 |
0.551 |
|
| 1983 |
Barton DHR, Motherwell WB, Zard SZ. A simple and economic synthesis of the corticosteroid side chain from 17-oxo-steroids. Improved ketone-nitromethane reactions Bulletin De La Societe Chimique De France. II-61-II-65. DOI: 10.1002/Chin.198343312 |
0.592 |
|
| 1982 |
Viger A, Marquet A, Barton DHR, Motherwell WB, Zard SZ. Stereochemistry of the reduction of 3β-benzoyloxycholest-5-en-4-one with sodium borohydride Journal of the Chemical Society-Perkin Transactions 1. 13: 1937-1940. DOI: 10.1039/P19820001937 |
0.527 |
|
| 1982 |
Barton DHR, Motherwell WB, Zard SZ. A simple construction of the hydroxy-ketone side chain of corticosteroids from 17-oxo-steroids via nitro-olefins Journal of the Chemical Society, Chemical Communications. 551-552. DOI: 10.1039/C39820000551 |
0.609 |
|
| 1982 |
Barton DHR, Motherwell WB, Zard SZ. A Simple Construction Of The Corticosteroid Side Chain From 17-Ketosteroids Cheminform. 13. DOI: 10.1002/Chin.198243336 |
0.517 |
|
| 1982 |
Barton DHR, Motherwell WB, Zard SZ. A Simple Construction Of The Hydroxy Ketone Side Chain Of Corticosteroids From 17-Oxo Steroids Via Nitro Olefins Cheminform. 13. DOI: 10.1002/Chin.198239350 |
0.584 |
|
| 1981 |
Barton DHR, Motherwell WB, Zard SZ. Efficient synthesis of the corticosteroid side-chain from 17-ketones Journal of the Chemical Society, Chemical Communications. 774-775. DOI: 10.1039/C39810000774 |
0.628 |
|
| 1981 |
Barton DHR, Motherwell WB, Zard SZ. Efficient Synthesis Of The Corticosteroid Side Chain From 17-Ketones Cheminform. 12. DOI: 10.1002/Chin.198151341 |
0.581 |
|
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