| Year |
Citation |
Score |
| 2022 |
Manchoju A, Zelli R, Wang G, Eymard C, Oo A, Nemer M, Prévost M, Kim B, Guindon Y. Nucleotide Analogues Bearing a C2' or C3'-Stereogenic All-Carbon Quaternary Center as SARS-CoV-2 RdRp Inhibitors. Molecules (Basel, Switzerland). 27. PMID 35056878 DOI: 10.3390/molecules27020564 |
0.371 |
|
| 2020 |
Cardinal-David B, Labbé M, Prévost M, Dostie S, Guindon Y. Diastereoselective and regioselective synthesis of adenosine thionucleoside analogues using an acyclic approach Canadian Journal of Chemistry. 98: 466-470. DOI: 10.1139/Cjc-2020-0049 |
0.36 |
|
| 2019 |
Lussier T, Manchoju A, Wang G, Dostie S, Foster S, Mochirian P, Prévost M, Guindon Y. Diastereoselective Synthesis of Arabino- and Ribo-like Nucleoside Analogues Bearing a Stereogenic C3' All-Carbon Quaternary Center. The Journal of Organic Chemistry. PMID 31729227 DOI: 10.1021/Acs.Joc.9B02550 |
0.782 |
|
| 2019 |
Becerril-Jiménez F, Lussier T, Leblanc L, Eymard C, Dostie S, Prévost M, Guindon Y. Photoredox Catalyzed Stereoselective Radical Reactions to Synthesize Nucleoside Analogues with a C2'-Stereogenic All-Carbon Quaternary Center. The Journal of Organic Chemistry. PMID 31638391 DOI: 10.1021/Acs.Joc.9B02374 |
0.785 |
|
| 2019 |
Simard RD, Joyal M, Gillard L, Di Censo G, Maharsy W, Beauregard J, Colarusso P, Patel KD, Prévost M, Nemer M, Guindon Y. Synthesis of Sialyl LewisX Glycomimetics Bearing a Bicyclic 3-O, 4-C-Fused Galactopyranoside Scaffold. The Journal of Organic Chemistry. PMID 31088084 DOI: 10.1021/Acs.Joc.9B01075 |
0.318 |
|
| 2019 |
Lussier T, Waltz M, Freure G, Mochirian P, Dostie S, Prévost M, Guindon Y. Synthesis of nucleoside analogues using acyclic diastereoselective reactions Arkivoc. 2019: 113-142. DOI: 10.24820/Ark.5550190.P010.832 |
0.784 |
|
| 2016 |
Dostie S, Prévost M, Mochirian P, Tanveer K, Andrella N, Rostami A, Tambutet G, Guindon Y. Diastereoselective Synthesis of C2'-Fluorinated Nucleoside Analogues using an Acyclic Approach. The Journal of Organic Chemistry. PMID 27736093 DOI: 10.1021/Acs.Joc.6B01845 |
0.421 |
|
| 2016 |
Tambutet G, Guindon Y. Diastereoselective Radical Hydrogen Transfer Reactions using N-Heterocyclic Carbene Boranes. The Journal of Organic Chemistry. PMID 27709943 DOI: 10.1021/Acs.Joc.6B02066 |
0.524 |
|
| 2015 |
Godin F, Mochirian P, St-Pierre G, Guindon Y. Total synthesis of zincophorin methyl ester. Stereocontrol of 1,2-induction using sterically hindered enoxysilanes Tetrahedron. 71: 709-726. DOI: 10.1016/j.tet.2014.11.061 |
0.402 |
|
| 2014 |
Tambutet G, Becerril-Jiménez F, Dostie S, Simard R, Prévost M, Mochirian P, Guindon Y. Dual-face nucleoside scaffold featuring a stereogenic all-carbon quaternary center. Intramolecular silicon tethered group-transfer reaction. Organic Letters. 16: 5698-701. PMID 25320862 DOI: 10.1021/Ol502777R |
0.447 |
|
| 2014 |
Prévost M, Dostie S, Waltz MÈ, Guindon Y. Investigation of diastereoselective acyclic α-alkoxydithioacetal substitutions involving thiacarbenium intermediates. The Journal of Organic Chemistry. 79: 10504-25. PMID 25280088 DOI: 10.1021/Jo502181A |
0.411 |
|
| 2014 |
Godin F, Duplessis M, Buonomano C, Trinh T, Houde K, Chapdelaine D, Rodrigue J, Boutros A, Guindon Y. Stereocontrolled synthesis of propionate motifs from l-lactic and l-alanine aldehydes. A DFT study of the hydrogen transfer under endocyclic control Organic Chemistry Frontiers. 1: 974-982. DOI: 10.1039/C4Qo00142G |
0.38 |
|
| 2013 |
Godin F, Prévost M, Gorelsky SI, Mochirian P, Nguyen M, Viens F, Guindon Y. Diastereoselective hydrogen-transfer reactions: an experimental and DFT study. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 9308-18. PMID 23733260 DOI: 10.1002/Chem.201300377 |
0.461 |
|
| 2013 |
Godin F, Prévost M, Viens F, Mochirian P, Brazeau JF, Gorelsky SI, Guindon Y. A study of exocyclic radical reductions of polysubstituted tetrahydropyrans. The Journal of Organic Chemistry. 78: 6075-103. PMID 23688058 DOI: 10.1021/Jo400721E |
0.448 |
|
| 2013 |
St-Jean O, Prévost M, Guindon Y. Study of the endocyclic versus exocyclic C-O bond cleavage pathways of α- and β-methyl furanosides. The Journal of Organic Chemistry. 78: 2935-46. PMID 23485332 DOI: 10.1021/Jo3027438 |
0.47 |
|
| 2012 |
Dostie S, Prévost M, Guindon Y. A stereoselective approach to β-L-arabino nucleoside analogues: synthesis and cyclization of acyclic 1',2'-syn N,O-acetals. The Journal of Organic Chemistry. 77: 7176-86. PMID 22873650 DOI: 10.1021/Jo3012754 |
0.442 |
|
| 2012 |
Godin F, Katsoulis I, Fiola-Masson E, Dhambri S, Mochirian P, Guindon Y. Stereodivergent synthesis of the C1-C9 tetrahydropyran subunit of zincophorin and isomers thereof Synthesis. 44: 474-488. DOI: 10.1055/S-0031-1289661 |
0.479 |
|
| 2012 |
Guindon Y, Godin F, Mochirian PA, Prévost M. 2.16 Selected Diastereoselective Reactions: Free Radical Additions and Cyclizations Comprehensive Chirality. 2: 472-503. DOI: 10.1016/B978-0-08-095167-6.00215-9 |
0.357 |
|
| 2011 |
Mochirian P, Godin F, Katsoulis I, Fontaine I, Brazeau JF, Guindon Y. A bidirectional approach to the synthesis of polypropionates: synthesis of C1-C13 fragment of zincophorin and related isomers. The Journal of Organic Chemistry. 76: 7654-76. PMID 21863874 DOI: 10.1021/Jo2013884 |
0.498 |
|
| 2010 |
Prévost M, St-Jean O, Guindon Y. Synthesis of 1',2'-cis-nucleoside analogues: evidence of stereoelectronic control for SN2 reactions at the anomeric center of furanosides. Journal of the American Chemical Society. 132: 12433-9. PMID 20704290 DOI: 10.1021/Ja104429Y |
0.425 |
|
| 2010 |
Brazeau JF, Guilbault AA, Kochuparampil J, Mochirian P, Guindon Y. Stereocontrolled synthesis of C1-C17 fragment of narasin via a free radical-based approach. Organic Letters. 12: 36-9. PMID 20035562 DOI: 10.1021/Ol902414U |
0.499 |
|
| 2010 |
GUINDON Y, YOAKIM C, GORYS V, OGILVIE WW, DELORME D, RENAUD J, ROBINSON G, LAVALLEE J, SLASSI A, JUNG G, RANCOURT J, DURKIN K, LIOTTA D. ChemInform Abstract: Stereoselective Hydrogen Transfer Reactions Involving Acyclic Radicals. Tandem Substituted Tetrahydrofuran Formation and Stereoselective Reduction: Synthesis of the C17-C22 Subunit of Ionomycin. Cheminform. 25: no-no. DOI: 10.1002/chin.199432248 |
0.43 |
|
| 2009 |
Chapdelaine D, Cardinal-David B, Prévost M, Gagnon M, Thumin I, Guindon Y. A stereoselective approach to nucleosides and 4'-thioanalogues from acyclic precursors. Journal of the American Chemical Society. 131: 17242-5. PMID 19902939 DOI: 10.1021/Ja905452F |
0.74 |
|
| 2009 |
Duplessis M, Waltz ME, Bencheqroun M, Cardinal-David B, Guindon Y. Stereoselective quaternary center construction via atom-transfer radical cyclization using silicon tethers on acyclic precursors. Organic Letters. 11: 3148-51. PMID 19552388 DOI: 10.1021/Ol901126Y |
0.792 |
|
| 2009 |
Denissova I, Maretti L, Wilkes BC, Scaiano JC, Guindon Y. Raising the ceiling of diastereoselectivity in hydrogen transfer on acyclic radicals. The Journal of Organic Chemistry. 74: 2438-46. PMID 19226157 DOI: 10.1021/Jo802634W |
0.425 |
|
| 2009 |
Brazeau JF, Mochirian P, Prévost M, Guindon Y. Stereopentads derived from a sequence of Mukaiyama aldolization and free radical reduction on alpha-methyl-beta-alkoxy aldehydes: a general strategy for efficient polypropionate synthesis. The Journal of Organic Chemistry. 74: 64-74. PMID 19063596 DOI: 10.1021/Jo8021583 |
0.493 |
|
| 2006 |
Cardinal-David B, Brazeau JF, Katsoulis IA, Guindon Y. Phenylselenoethers as precursors of acyclic free radicals. Creating tertiary and quaternary centers using free radical-based intermediates Current Organic Chemistry. 10: 1939-1961. DOI: 10.2174/138527206778521259 |
0.747 |
|
| 2005 |
Cardinal-David B, Guérin B, Guindon Y. Synthesis of tertiary and quaternary stereogenic centers: a diastereoselective tandem reaction sequence combining Mukaiyama and free radical-based allylation. The Journal of Organic Chemistry. 70: 776-84. PMID 15675832 DOI: 10.1021/Jo048687J |
0.8 |
|
| 2005 |
Guindon Y, Bencheqroun M, Bouzide A. Synthesis of postulated molecular probes: stereoselective free-radical-mediated C-glycosylation in tandem with hydrogen transfer. Journal of the American Chemical Society. 127: 554-8. PMID 15643879 DOI: 10.1021/Ja046389Y |
0.505 |
|
| 2004 |
Guindon Y, Brazeau JF. Diastereoselective mukaiyama and free radical processes for the synthesis of polypropionate units. Organic Letters. 6: 2599-602. PMID 15255700 DOI: 10.1021/Ol049086H |
0.554 |
|
| 2003 |
Guindon Y, Ogilvie WW, Bordeleau J, Cui WL, Durkin K, Gorys V, Juteau H, Lemieux R, Liotta D, Simoneau B, Yoakim C. Opening of tartrate acetals using dialkylboron bromide: evidence for stereoselectivity downstream from ring fission. Journal of the American Chemical Society. 125: 428-36. PMID 12517155 DOI: 10.1021/Ja012530G |
0.44 |
|
| 2002 |
Guindon Y, Prévost M, Mochirian P, Guérin B. Synthesis of 2,3-anti-3,4-anti and 2,3-anti-3,4-syn propionate motifs: a diastereoselective tandem sequence of Mukaiyama and free-radical-based hydrogen transfer reactions. Organic Letters. 4: 1019-22. PMID 11893211 DOI: 10.1021/Ol025605+ |
0.49 |
|
| 2002 |
Guindon Y, Gagnon M, Thumin I, Chapdelaine D, Jung G, Guérin B. Synthesis of N-glycosides. An alternative approach based on diastereoselective base coupling and S(N)2 cyclization. Organic Letters. 4: 241-4. PMID 11796060 DOI: 10.1021/Ol016991I |
0.389 |
|
| 2002 |
Guindon Y, Houde K, Prévost M, Cardinal-David B, Landry SR, Daoust B, Bencheqroun aM, Guérin B. Synthesis of Propionate Motifs: Diastereoselective Tandem Reactions Involving Anionic and Free Radical Based Processes [J. Am. Chem. Soc. 2001, 123 (35), 8496−8501]. Journal of the American Chemical Society. 124: 168-168. DOI: 10.1021/Ja015131U |
0.495 |
|
| 2002 |
Mochirian P, Cardinal-David B, Guérin B, Prévost M, Guindon Y. Synthesis of polypropionate motifs containing the anti-anti unit Tetrahedron Letters. 43: 7067-7071. DOI: 10.1016/S0040-4039(02)01557-5 |
0.769 |
|
| 2001 |
Guindon Y, Soucy F, Yoakim C, Ogilvie WW, Plamondon L. Diastereoselective synthesis of 2,3,5-trisubstituted tetrahydrofurans via cyclofunctionalization reactions. Evidence of stereoelectronic effects. The Journal of Organic Chemistry. 66: 8992-6. PMID 11749632 DOI: 10.1021/Jo010873R |
0.469 |
|
| 2001 |
Guindon Y, Houde K, Prévost M, Cardinal-David B, Landry SR, Daoust B, Bencheqroun M, Guérin B. Synthesis of propionate motifs: diastereoselective tandem reactions involving anionic and free radical based processes. Journal of the American Chemical Society. 123: 8496-501. PMID 11525656 DOI: 10.1021/Ja010805M |
0.792 |
|
| 2001 |
Guindon Y, Murtagh L, Caron V, Landry SR, Jung G, Bencheqroun M, Faucher AM, Guérin B. Cyclofunctionalization and free-radical-based hydrogen-transfer reactions. An iterative reaction sequence applied to the synthesis of the C(7)-C(16) subunit of zincophorin. The Journal of Organic Chemistry. 66: 5427-37. PMID 11485466 DOI: 10.1021/Jo010310F |
0.483 |
|
| 2001 |
Guindon Y, Guérin B, Landry SR. Intramolecular aminyl and iminyl radical additions to alpha,beta-unsaturated esters. Diastereoselective tandem cyclofunctionalization and hydrogen transfer reactions. Organic Letters. 3: 2293-6. PMID 11463299 DOI: 10.1021/Ol0160809 |
0.486 |
|
| 2001 |
Bouvier JP, Jung G, Liu Z, Guérin B, Guindon Y. Stereocontrol in radical processes through the exocyclic effect: dual role of triethylboron as radical initiator and in situ derivatization agent. Organic Letters. 3: 1391-4. PMID 11348242 DOI: 10.1021/Ol015758H |
0.432 |
|
| 2001 |
Guindon Y, Slassi A, Bencheqroun M. Corrigendum to “Influence of N-substituted lactams on acyclic free radical based hydrogen transfer” Tetrahedron Letters. 42: 8741. DOI: 10.1016/S0040-4039(01)01838-X |
0.354 |
|
| 2001 |
Guindon Y, Bencheqroun M. Influence of N-substituted lactams on acyclic free radical based hydrogen transfer Tetrahedron Letters. 42: 6041-6044. DOI: 10.1016/S0040-4039(01)01213-8 |
0.439 |
|
| 2000 |
Guerin B, Chabot C, Mackintosh N, Ogilvie WW, Guindon Y. Free radicals and Lewis acid. Chelation-controlled radical allylations of substituted α-halo- or α- phenylseleno-β-alkoxy esters. The endocyclic effect Canadian Journal of Chemistry. 78: 852-867. DOI: 10.1139/V00-074 |
0.506 |
|
| 1998 |
Guindon Y, Jung G, Guérin B, Ogilvie WW. Hydrogen and allylation transfer reactions in acyclic free radicals Synlett. 213-220. DOI: 10.1055/S-1998-1618 |
0.465 |
|
| 1998 |
Guindon Y, Rancourt J. The Use of Lewis Acids in Radical Chemistry. Chelation-Controlled Radical Reductions of Substituted α-Bromo-β-alkoxy Esters and Chelation-Controlled Radical Addition Reactions Journal of Organic Chemistry. 63: 6554-6565. DOI: 10.1021/Jo980636X |
0.497 |
|
| 1998 |
Guindon Y, Denis RC. Intramolecular oxygen radical additions to α,β-unsaturated esters. Diastereoselective tandem cyclofunctionalization and hydrogen transfer reactions Tetrahedron Letters. 39: 339-342. DOI: 10.1016/S0040-4039(97)10515-9 |
0.506 |
|
| 1997 |
Guindon Y, Faucher AM, Bourque E, Caron V, Jung G, Landry SR. The Exocyclic Effect: Protecting Group Strategy to Enhance Stereoselectivity in Hydrogen Transfer Reactions of Acyclic Free Radicals Journal of Organic Chemistry. 62: 9276-9283. DOI: 10.1021/Jo971595S |
0.461 |
|
| 1997 |
Beaulieu PL, Lavallée P, Abraham A, Anderson PC, Boucher C, Bousquet Y, Duceppe JS, Gillard J, Gorys V, Grand-Maître C, Grenier L, Guindon Y, Guse I, Plamondon L, Soucy F, et al. Practical, stereoselective synthesis of palinavir, a potent HIV protease inhibitor Journal of Organic Chemistry. 62: 3440-3448. DOI: 10.1021/Jo9702655 |
0.321 |
|
| 1997 |
Guindon Y, Liu Z, Jung G. The Exo-Cyclic Effect: Strategy Employingin SituDerivatization or Lewis Acid Complexation to Enhance Stereoselectivity in Hydrogen Transfer Reactions Journal of the American Chemical Society. 119: 9289-9290. DOI: 10.1021/Ja972064O |
0.409 |
|
| 1996 |
Guindon Y, Guérin B, Rancourt J, Chabot C, Mackintosh N, Ogilvie WW. Lewis acids in diastereoselective processes involving acyclic radicals Pure and Applied Chemistry. 68: 89-96. DOI: 10.1351/Pac199668010089 |
0.484 |
|
| 1996 |
Guindon Y, Guérin B, Chabot C, Ogilvie W. Stereoselective radical carbon-carbon bond forming reactions of β-alkoxy esters: Atom and group transfer allylations under bidentate chelation controlled conditions Journal of the American Chemical Society. 118: 12528-12535. DOI: 10.1021/Ja9541241 |
0.496 |
|
| 1995 |
Guindon Y, Guérin B, Chabot C, Mackintosh N, Ogilvie WW. Stereoselective Radical Allylation of α-Iodo-β-Alkoxy Esters: Reversal of Facial Selectivity by Lewis Acid Complexation Synlett. 1995: 449-451. DOI: 10.1055/S-1995-4995 |
0.353 |
|
| 1995 |
Guindon Y, Slassi A, Rancourt J, Bantle G, Bencheqroun M, Murtagh L, Ghiro E, Jung G. Role of σ-donation in the stereocontrol of hydrogen-transfer reactions involving acyclic radicals Journal of Organic Chemistry. 60: 288-289. |
0.315 |
|
| 1994 |
Guindon Y, Yoakim C, Gorys V, Ogilvie WW, Delorme D, Renaud J, Robinson G, Lavallée JF, Slassi A, Jung G, Rancourt J, Durkin K, Liotta D. Stereoselective hydrogen transfer reactions involving acyclic radicals. Tandem substituted tetrahydrofuran formation and stereoselective reduction: Synthesis of the C17-C22 subunit of ionomycin Journal of Organic Chemistry. 59: 1166-1178. DOI: 10.1021/Jo00084A040 |
0.548 |
|
| 1993 |
Giese B, Damm W, Wetterich F, Zeitz HG, Rancourt J, Guindon Y. The effect of polar substituents on the conformation and stereochemistry of enolate radicals Tetrahedron Letters. 34: 5885-5888. DOI: 10.1016/S0040-4039(00)73805-6 |
0.369 |
|
| 1992 |
Durkin K, Liotta D, Rancourt J, Lavallee JF, Boisvert L, Guindon Y. Stereoselective hydrogen-transfer reactions involving acyclic radicals. A study of radical conformations using semiempirical calculations Journal of the American Chemical Society. 114: 4912-4914. DOI: 10.1021/Ja00038A072 |
0.44 |
|
| 1992 |
Guindon Y, Slassi A, Ghiro E, Bantle G, Jung G. Stereoselective silver triflate-mediated iodocyclization of carbamates Tetrahedron Letters. 33: 4257-4260. DOI: 10.1016/S0040-4039(00)74232-8 |
0.362 |
|
| 1992 |
Durkin K, Liotta D, Rancourt J, Lavallee JF, Boisvert L, Guindon Y. Stereoselective hydrogen-transfer reactions involving acyclic radicals. A study of radical conformations using semiempirical calculations Journal of the American Chemical Society. 114: 4912-4914. |
0.333 |
|
| 1991 |
Guindon Y, Lavallee JF, Llinas-Brunet M, Horner G, Rancourt J. Stereoselective chelation-controlled reduction of .alpha.-iodo-.beta.-alkoxy esters under radical conditions Journal of the American Chemical Society. 113: 9701-9702. DOI: 10.1021/Ja00025A061 |
0.32 |
|
| 1991 |
Guindon Y, Lavallée JF, Boisvert L, Chabot C, Delorme D, Yoakim C, Hall D, Lemieux R, Simoneau B. Stereoselective rardical-mediated reduction and alkylation of α-halo esters Tetrahedron Letters. 32: 27-30. DOI: 10.1016/S0040-4039(00)71209-3 |
0.373 |
|
| 1991 |
Guindon Y, Simoneaua B, Yoakima C, Gorysa V, Lemieuxa R, Ogilvie W. Stereoselective opening of acetals derived from dimethyl tartrate Tetrahedron Letters. 32: 5453-5456. DOI: 10.1016/0040-4039(91)80056-C |
0.37 |
|
| 1990 |
Guindon Y, Girard Y, Berthiaume S, Gorys V, Lemieux R, Yoakim C. Dialkyl and diaryl boron halides: reductive opening of benzylidene acetals Canadian Journal of Chemistry. 68: 897-902. DOI: 10.1139/V90-141 |
0.441 |
|
| 1990 |
Guindon Y, Yoakim C, Lemieux R, Boisvert L, Delorme D, Lavallée JF. Stereoselective reduction of acyclic α-bromo esters Tetrahedron Letters. 31: 2845-2848. DOI: 10.1016/0040-4039(90)80163-G |
0.37 |
|
| 1989 |
Labelle M, Guindon Y. Diastereoselective synthesis of 2,3-disubstituted tetrahydrofuran synthons via the iodoetherification reaction. A transition state model based rationalization of the allylic asymmetric induction Journal of the American Chemical Society. 111: 2204-2210. DOI: 10.1021/Ja00188A039 |
0.427 |
|
| 1988 |
Gillard JW, Fortin R, Morton HE, Yoakim C, Quesnelle CA, Daignault S, Guindon Y. Symmetrical alkoxysilyl ethers. A new class of alcohol-protecting groups. Preparation of tert-butoxydiphenylsilyl ethers Journal of Organic Chemistry. 53: 2602-2608. DOI: 10.1021/Jo00246A038 |
0.311 |
|
| 1988 |
Guindon Y, Delorme D, Lau CK, Zamboni R. Total synthesis of LTB4 and analogs Journal of Organic Chemistry. 53: 267-275. DOI: 10.1021/Jo00237A008 |
0.388 |
|
| 1988 |
Labelle M, Morton HE, Guindon Y, Springer JP. Homoallylic chiral induction in the synthesis of 2,4-disubstituted tetrahydrofurans by iodoetherification. Synthetic scope and chiral induction mechanism Journal of the American Chemical Society. 110: 4533-4540. DOI: 10.1021/Ja00222A008 |
0.438 |
|
| 1988 |
Guindon Y, Delorme D, Lau CK, Zamboni R. Total synthesis of LTB4 and analogues Journal of Organic Chemistry. 53: 267-275. |
0.384 |
|
| 1987 |
Guindon Y, Delorme D. Total synthesis of leukotriene B4 analogues: 3-thia-LTB4 and 3-thia-20,20,20-trifluoro-LTB4 Canadian Journal of Chemistry. 65: 1438-1440. DOI: 10.1139/V87-244 |
0.366 |
|
| 1987 |
Guindon Y, Therien M, Girard Y, Yoakim C. Regiocontrolled opening of cyclic ethers using dimethylboron bromide Journal of Organic Chemistry. 52: 1680-1686. DOI: 10.1021/Jo00385A007 |
0.375 |
|
| 1987 |
Gauthier JY, Guindon Y. Exceptionally mild and stereospecific ring fragmentations promoted by dimethylboron bromide Tetrahedron Letters. 28: 5985-5988. DOI: 10.1016/S0040-4039(00)96843-6 |
0.348 |
|
| 1987 |
Guindon Y, Bernstein MA, Anderson PC. Ring cleavage of THP and THF ethers using dimethylboron bromide Tetrahedron Letters. 28: 2225-2228. DOI: 10.1016/S0040-4039(00)96086-6 |
0.471 |
|
| 1987 |
Guindon Y, Anderson PC. Stereoelectronic effects in the ring cleavage of methyl glycopyranosides using dimethylboron bromide Tetrahedron Letters. 28: 2485-2488. DOI: 10.1016/S0040-4039(00)95447-9 |
0.379 |
|
| 1986 |
Bernstein MA, Morton HE, Guindon Y. A general method for determining the anomeric configuration of C-furanoside derivatives: A 1H nuclear magnetic resonance nuclear Overhauser effect study Journal of the Chemical Society, Perkin Transactions 2. 1155-1163. DOI: 10.1039/P29860001155 |
0.334 |
|
| 1986 |
Guindon Y, Denis YS, Daigneault S, Morton HE. Synthetic utility of chiral tetrahydrofurans: Preparation of (1R, 3R, 5S)-1, 3-dimethyl-2, 9-dioxabicyclo[3.3.1]nonane Tetrahedron Letters. 27: 1237-1240. DOI: 10.1016/S0040-4039(00)84226-4 |
0.325 |
|
| 1986 |
Hanessian S, Guindon Y, Lavallee P, Dextraze P. Total Synthesis of 11‐Oxaprostaglandin F2α and F2β. Cheminform. 17. DOI: 10.1002/Chin.198606321 |
0.525 |
|
| 1985 |
Morton HE, Guindon Y. Dimethylboron bromide--interconversion of protecting groups: preparation of MTM [(methylthio)methyl] ethers, O,S-acetals, and cyanomethyl ethers The Journal of Organic Chemistry. 50: 5379-5382. DOI: 10.1021/Jo00225A077 |
0.306 |
|
| 1985 |
Guindon Y, Yoakim C, Bernstein MA, Morton HE. Preparation of ethyl 5(s),6-epoxy-3(r)-(methoxymethoxy)hexanoate: a key chiral intermediate for mevinolin and compactin Tetrahedron Letters. 26: 1185-1188. DOI: 10.1016/S0040-4039(00)98429-6 |
0.367 |
|
| 1985 |
Hanessian S, Guindon Y, Lavallée P, Dextraze P. Total synthesis of 11-oxaprostaglandin F2α and F2β Carbohydrate Research. 141: 221-238. DOI: 10.1016/S0008-6215(00)90454-3 |
0.552 |
|
| 1984 |
Guindon Y, Yoakim C, Morton HE. Dimethylboron bromide and diphenylboron bromide: cleavage of acetals and ketals The Journal of Organic Chemistry. 49: 3912-3920. DOI: 10.1021/jo00195a007 |
0.315 |
|
| 1984 |
Guindon Y, Atkinson JG, Morton HE. Deoxygenation of sulfoxides with boron bromide reagents Journal of Organic Chemistry. 49: 4538-4540. DOI: 10.1002/Chin.198516147 |
0.47 |
|
| 1984 |
Guindon Y, Yoakim C, Morton HE. Dimethylboron bromide and diphenylboron bromide: Cleavage of acetals and ketals Journal of Organic Chemistry. 49: 3912-3920. DOI: 10.1002/Chin.198514107 |
0.464 |
|
| 1983 |
Guindon Y, Yoakim C, Morton HE. Cleavage of carbonoxygen bonds. Dimethylboron bromide. A new reagent for ether cleavage Tetrahedron Letters. 24: 2969-2972. DOI: 10.1016/S0040-4039(00)88071-5 |
0.395 |
|
| 1982 |
Guindon Y, Zamboni R, Lau CK, Rokach J. Stereospecific synthesis of leukotriene B4 (LTB4) Tetrahedron Letters. 23: 739-742. DOI: 10.1016/S0040-4039(00)86935-X |
0.359 |
|
| 1981 |
Guindon Y, Young RN, Frenette R. Synthesis of β-Trimethylsilyloxythioethers and β-Hydroxythioethers by the Reaction of Epoxides with Aryl- and Alkylthiotrimethylsilanes Synthetic Communications. 11: 391-398. DOI: 10.1080/00397918108064305 |
0.461 |
|
| 1981 |
Young RN, Coombs W, Guindon Y, Rokach J, Ethier D, Hall R. The preparation of octahydro leukotrienes C, D, and E via a stereoselective sulfenyllactonization reaction Tetrahedron Letters. 22: 4933-4936. DOI: 10.1016/S0040-4039(01)92385-8 |
0.434 |
|
| 1981 |
Rokach J, Lau CK, Zamboni R, Guindon Y. A C-glycoside route to leukotrienes Tetrahedron Letters. 22: 2763-2766. DOI: 10.1016/S0040-4039(01)90546-5 |
0.372 |
|
| 1981 |
Rokach J, Zamboni R, Lau CK, Guindon Y. The stereospecific synthesis of leukotriene A4 (LTA4), 5-epi-LTA4, 6-epi-LTA4 and 5-epi,6-epi-LTA4 Tetrahedron Letters. 22: 2759-2762. DOI: 10.1016/S0040-4039(01)90545-3 |
0.375 |
|
| 1980 |
Rokach J, Girard Y, Guindon Y, Atkinson JG, Larue M, Young RN, Masson P, Holme G. The synthesis of a leukotriene with SRS-like activity Tetrahedron Letters. 21: 1485-1488. DOI: 10.1016/S0040-4039(00)92753-9 |
0.358 |
|
| 1980 |
Hanessian S, Guindon Y. Cleavage of methyl and benzyl ethers with thiotrimethylsilanes Tetrahedron Letters. 21: 2305-2308. DOI: 10.1016/S0040-4039(00)92591-7 |
0.5 |
|
| 1980 |
Hanessian S, Guindon Y. Chemistry of the glycosidic linkage. Direct conversion of glycosides into 1-thioglycosides by use of [alkyl(or aryl)thio]trimethylsilanes Carbohydrate Research. 86: C3-C6. DOI: 10.1016/S0008-6215(00)85913-3 |
0.54 |
|
| 1978 |
Hanessian S, Rancourt G, Guindon Y. Assembly of the carbon skeletal framework of erythronolide A Canadian Journal of Chemistry. 56: 1843-1846. DOI: 10.1139/V78-299 |
0.505 |
|
| 1975 |
HANESSIAN S, DEXTRAZE P, FOUGEROUSSE A, GUINDON Y. ChemInform Abstract: STERISCH KONTROLLIERTE SYNTHESE VON CHIRALEN VORLAEUFERN DER 11-OXAPROSTAGLANDINE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197506458 |
0.481 |
|
| 1974 |
Hanessian S, Dextraze P, Fougerousse A, Guindon Y. Synthese stereocontrolee des precurseurs chiraux des 11-oxaprostaglandines Tetrahedron Letters. 15: 3983-3986. DOI: 10.1016/S0040-4039(01)92063-5 |
0.424 |
|
| 1974 |
Hanessian S, Ogawa T, Guindon Y, Kamennof JL, Roy R. Utilization of functionalized polymers in synthesis: immobilization of carbohydrates as acetals, and some chemical transformations Carbohydrate Research. 38: C15-C18. DOI: 10.1016/S0008-6215(00)82382-4 |
0.445 |
|
| 1974 |
Hanessian S, Ogawa T, Guindon Y. Facile access to ethyl 2-C-β-D-ribofuranosylacetates Carbohydrate Research. 38: C12-C14. DOI: 10.1016/S0008-6215(00)82381-2 |
0.448 |
|
| Show low-probability matches. |