Year |
Citation |
Score |
2022 |
Rowshanpour R, Gravel M, Dudding T. N-Heterocyclic Carbene Organocatalyzed Redox-Active/Ring Expansion Reactions: Mechanistic Insights Unveiling Base Cooperativity. The Journal of Organic Chemistry. PMID 36450122 DOI: 10.1021/acs.joc.2c02462 |
0.344 |
|
2022 |
Langdon SM, Gravel M. An Alternative Method for the Synthesis of -Pentafluorophenyl Triazolium Salts. Organic Letters. PMID 36169221 DOI: 10.1021/acs.orglett.2c02863 |
0.421 |
|
2021 |
Parmar K, Haghshenas P, Gravel M. Total Synthesis of (+)-Hyacinthacine A Using a Chemoselective Cross-Benzoin Reaction and a Furan Photooxygenation-Amine Cyclization Strategy. Organic Letters. PMID 33538602 DOI: 10.1021/acs.orglett.1c00090 |
0.517 |
|
2020 |
Rezazadeh Khalkhali M, Wilde MMD, Gravel M. Enantioselective Stetter Reactions Catalyzed by Bis(amino)cyclopropenylidenes: Important Role for Water as an Additive. Organic Letters. PMID 33320678 DOI: 10.1021/acs.orglett.0c03879 |
0.529 |
|
2019 |
Duan A, Fell JS, Yu P, Lam CY, Gravel M, Houk KN. Theoretical Study of Diastereoselective NHC-Catalyzed Cross-Benzoin Reactions between Furfural and N-Boc-Protected α-Amino Aldehydes. The Journal of Organic Chemistry. PMID 31512872 DOI: 10.1021/Acs.Joc.9B01821 |
0.454 |
|
2018 |
Garapati VKR, Gravel M. Oxazolium Salts as Organocatalysts for the Umpolung of Aldehydes. Organic Letters. PMID 30270631 DOI: 10.1021/Acs.Orglett.8B02636 |
0.531 |
|
2018 |
Curtin BH, Manoni F, Park J, Sisto LJ, Lam YH, Gravel M, Roulston A, Harran PG. Assembly of complex macrocycles by incrementally amalgamating unprotected peptides with a designed four-armed insert. The Journal of Organic Chemistry. PMID 29494773 DOI: 10.1021/Acs.Joc.7B02958 |
0.311 |
|
2017 |
Gravel M, Haghshenas P, Langdon S. Thieme Chemistry Journals Awardees – Where Are They Now? Carbene Organocatalysis for Stetter, Benzoin, Domino, and Ring-Expansion Reactions Synlett. 28: 542-559. DOI: 10.1055/S-0036-1588675 |
0.622 |
|
2016 |
Haghshenas P, Quail JW, Gravel M. Substrate-Controlled Diastereoselectivity Reversal in NHC-Catalyzed Cross-Benzoin Reactions Using N-Boc-N-Bn-Protected α-Amino Aldehydes. The Journal of Organic Chemistry. 81: 12075-12083. PMID 27978724 DOI: 10.1021/Acs.Joc.6B02568 |
0.536 |
|
2016 |
Haghshenas P, Gravel M. Chemo- and Diastereoselective N-Heterocyclic Carbene-Catalyzed Cross-Benzoin Reactions Using N-Boc-α-amino Aldehydes. Organic Letters. PMID 27574804 DOI: 10.1021/Acs.Orglett.6B02123 |
0.56 |
|
2016 |
Turkmen YE, Gravel M, Rawal VH. Studies Directed toward the Synthesis of Aspidophytine: Construction of its Perhydroquinoline Core. The Journal of Organic Chemistry. PMID 27525506 DOI: 10.1021/Acs.Joc.6B01574 |
0.761 |
|
2015 |
Langdon SM, Legault CY, Gravel M. Origin of chemoselectivity in N-heterocyclic carbene catalyzed cross-benzoin reactions: DFT and experimental insights. The Journal of Organic Chemistry. 80: 3597-610. PMID 25734574 DOI: 10.1021/Acs.Joc.5B00301 |
0.519 |
|
2015 |
Langdon SM, Legault CY, Gravel M. Origin of chemoselectivity in N-heterocyclic carbene catalyzed cross-benzoin reactions: DFT and experimental insights Journal of Organic Chemistry. 80: 3597-3610. DOI: 10.1021/acs.joc.5b00301 |
0.441 |
|
2014 |
Wilde MM, Gravel M. Bis(amino)cyclopropenylidene (BAC) catalyzed aza-benzoin reaction. Organic Letters. 16: 5308-11. PMID 25272948 DOI: 10.1021/Ol5024807 |
0.631 |
|
2014 |
Langdon SM, Wilde MM, Thai K, Gravel M. Chemoselective N-heterocyclic carbene-catalyzed cross-benzoin reactions: importance of the fused ring in triazolium salts. Journal of the American Chemical Society. 136: 7539-42. PMID 24809936 DOI: 10.1021/Ja501772M |
0.616 |
|
2014 |
Wilde MMD, Gravel M. Bis(amino)cyclopropenylidene (BAC) catalyzed aza-benzoin reaction Organic Letters. 16: 5308-5311. DOI: 10.1021/ol5024807 |
0.549 |
|
2014 |
Langdon SM, Wilde MMD, Thai K, Gravel M. Chemoselective N-heterocyclic carbene-catalyzed cross-benzoin reactions: Importance of the fused ring in triazolium salts Journal of the American Chemical Society. 136: 7539-7542. DOI: 10.1021/ja501772m |
0.456 |
|
2014 |
Gravel M, Holmes JM. Stetter Reaction Comprehensive Organic Synthesis: Second Edition. 4: 1384-1406. DOI: 10.1016/B978-0-08-097742-3.00429-8 |
0.5 |
|
2014 |
Wilde MMD, Gravel M. Corrigendum: Bis(amino)cyclopropenylidenes as Organocatalysts for Acyl Anion and Extended Umpolung Reactions Angewandte Chemie International Edition. 53: 912-912. DOI: 10.1002/Anie.201310666 |
0.592 |
|
2013 |
Wilde MM, Gravel M. Bis(amino)cyclopropenylidenes as organocatalysts for acyl anion and extended umpolung reactions. Angewandte Chemie (International Ed. in English). 52: 12651-4. PMID 24123480 DOI: 10.1002/Anie.201307167 |
0.592 |
|
2013 |
Thai K, Langdon SM, Bilodeau F, Gravel M. Highly chemo- and enantioselective cross-benzoin reaction of aliphatic aldehydes and α-ketoesters. Organic Letters. 15: 2214-7. PMID 23607338 DOI: 10.1021/Ol400769T |
0.561 |
|
2013 |
Thai K, Langdon SM, Bilodeau F, Gravel M. Highly chemo- and enantioselective cross-benzoin reaction of aliphatic aldehydes and α-ketoesters Organic Letters. 15: 2214-2217. DOI: 10.1021/ol400769t |
0.43 |
|
2013 |
Wilde MMD, Gravel M. Bis(amino)cyclopropenylidenes as organocatalysts for acyl anion and extended umpolung reactions Angewandte Chemie - International Edition. 52: 12651-12654. DOI: 10.1002/anie.201307167 |
0.52 |
|
2012 |
Zhou S, Sánchez-Larios E, Gravel M. Scalable synthesis of highly reactive 1,3-diamino dienes from vinamidinium salts and their use in Diels-Alder reactions. The Journal of Organic Chemistry. 77: 3576-82. PMID 22397369 DOI: 10.1021/Jo202655H |
0.583 |
|
2012 |
Zhou S, Sánchez-Larios E, Gravel M. Scalable synthesis of highly reactive 1,3-diamino dienes from vinamidinium salts and their use in Diels-Alder reactions Journal of Organic Chemistry. 77: 3576-3582. DOI: 10.1021/jo202655h |
0.528 |
|
2011 |
Sánchez-Larios E, Thai K, Bilodeau F, Gravel M. Highly enantioselective intermolecular stetter reactions of β-aryl acceptors: α-ketoester moiety as handle for activation and synthetic manipulations Organic Letters. 13: 4942-4945. PMID 21846082 DOI: 10.1021/Ol202040B |
0.43 |
|
2011 |
Sánchez-Larios E, Holmes JM, Daschner CL, Gravel M. Synthesis of spiro bis-indanes via domino Stetter-aldol-Michael and Stetter-aldol-aldol reactions: Scope and limitations Synthesis. 1896-1904. DOI: 10.1055/S-0030-1260031 |
0.561 |
|
2011 |
Gravel M, Thai K, Wang L, Dudding T, Bilodeau F. NHC-Catalyzed Intramolecular Redox Lactamization Synfacts. 2011: 0213-0213. DOI: 10.1055/S-0030-1259351 |
0.421 |
|
2010 |
Sánchez-Larios E, Holmes JM, Daschner CL, Gravel M. NHC-catalyzed spiro bis-indane formation via domino stetter - Aldol - Michael and stetter - Aldol - Aldol reactions Organic Letters. 12: 5772-5775. PMID 21090705 DOI: 10.1021/Ol102685U |
0.488 |
|
2010 |
Thai K, Wang L, Dudding T, Bilodeau F, Gravel M. NHC-Catalyzed intramolecular redox amidation for the synthesis of functionalized lactams Organic Letters. 12: 5708-5711. PMID 21080709 DOI: 10.1021/Ol102536S |
0.555 |
|
2010 |
Thai K, Gravel M. Design, synthesis, and application of chiral electron-poor guanidines as hydrogen-bonding catalysts for the Michael reaction Tetrahedron Asymmetry. 21: 751-755. DOI: 10.1016/J.Tetasy.2010.04.033 |
0.478 |
|
2009 |
Sánchez-Larios E, Gravel M. Diastereoselective synthesis of indanes via a domino Stetter-Michael reaction Journal of Organic Chemistry. 74: 7536-7539. PMID 19778082 DOI: 10.1021/Jo901468H |
0.596 |
|
2009 |
Holmes JM, Albert AL, Gravel M. Practical synthesis and highly diastereoselective Diels-Alder reactions of 1-alkylthio-3-silyloxybutadienes. The Journal of Organic Chemistry. 74: 6406-9. PMID 19627130 DOI: 10.1021/Jo901347U |
0.604 |
|
2009 |
Wang L, Thai K, Gravel M. NHC-catalyzed ring expansion of oxacycloalkane-2-carboxaldehydes: a versatile synthesis of lactones. Organic Letters. 11: 891-3. PMID 19199765 DOI: 10.1021/Ol8029005 |
0.506 |
|
2009 |
Wang L, Thai K, Gravel M. NHC-catalyzed ring expansion of oxacycloalkane-2-carboxaldehydes: A versatile synthesis of lactones Organic Letters. 11: 891-893. DOI: 10.1021/ol8029005 |
0.302 |
|
2009 |
Holmes JM, Albert AL, Gravel M. Practical synthesis and highly diastereoselective diels-alder reactions of 1-alkylthio-3-silyloxybutadienes Journal of Organic Chemistry. 74: 6406-6409. DOI: 10.1021/jo901347u |
0.515 |
|
2009 |
Thai K, Clement CW, Gravel M. A simple one-pot synthesis of triflyl guanidines: Access to highly substituted electron-poor guanidines Tetrahedron Letters. 50: 6540-6542. DOI: 10.1016/J.Tetlet.2009.09.040 |
0.458 |
|
2005 |
Gondi VB, Gravel M, Rawal VH. Hydrogen bond catalyzed enantioselective vinylogous Mukaiyama aldol reaction. Organic Letters. 7: 5657-60. PMID 16321015 DOI: 10.1021/Ol052301P |
0.71 |
|
2005 |
Gravel M, Toure BB, Hall DG. Practical Procedure for the Preparation of Functionalized (E)-1-Alkenylboronic Acids Including the Unprecedented 1-Alkoxycarbonyl Derivatives. Cheminform. 36. DOI: 10.1080/00304940409355974 |
0.658 |
|
2005 |
Rawal V, Gondi V, Gravel M. Organocatalytic Asymmetric Vinylogous Mukaiyama Aldol Reaction Synfacts. 2006: 0079-0079. DOI: 10.1055/S-2005-921719 |
0.719 |
|
2004 |
Hall DG, Gravel M, Lachance H, Lu X. Scope and Limitations of the Scandium-Catalyzed Enantioselective Addition of Chiral Allylboronates to Aldehydes Synthesis. 2004: 1290-1302. DOI: 10.1055/S-2004-822359 |
0.588 |
|
2004 |
Gravel M, Hall DG. DEAM-PS: Solid-Phase Chemistry for Boronic Acids Cheminform. 35. DOI: 10.1002/chin.200434284 |
0.434 |
|
2004 |
Gravel M, Lachance H, Lu X, Hall DG. Scope and limitations of the scandium-catalyzed enantioselective addition of chiral allylboronates to aldehydes Synthesis. 1290-1302. |
0.356 |
|
2003 |
Lachance H, Lu X, Gravel M, Hall DG. Scandium-catalyzed allylboration of aldehydes as a practical method for highly diastereo- and enantioselective construction of homoallylic alcohols. Journal of the American Chemical Society. 125: 10160-1. PMID 12926924 DOI: 10.1021/Ja036807J |
0.55 |
|
2002 |
Gravel M, Thompson KA, Zak M, Bérubé C, Hall DG. Universal solid-phase approach for the immobilization, derivatization, and resin-to-resin transfer reactions of boronic acids. The Journal of Organic Chemistry. 67: 3-15. PMID 11777432 DOI: 10.1021/Jo0106501 |
0.624 |
|
2000 |
Gravel M, Berube CD, Hall DG. Resin-to-resin suzuki coupling of solid supported arylboronic acids Journal of Combinatorial Chemistry. 2: 228-31. PMID 10827927 DOI: 10.1021/Cc990082R |
0.5 |
|
1999 |
Hall DG, Tailor J, Gravel M. N,N-Diethanolaminomethyl Polystyrene: An Efficient Solid Support to Immobilize Boronic Acids. Angewandte Chemie (International Ed. in English). 38: 3064-3067. PMID 10540423 DOI: 10.1002/(Sici)1521-3773(19991018)38:20<3064::Aid-Anie3064>3.0.Co;2-T |
0.543 |
|
1999 |
Hall DG, Tailor J, Gravel M. N,N-Diethanolaminomethylpolystyrol: ein effizienter fester Träger für die Immobilisierung von Boronsäuren Angewandte Chemie. 111: 3250-3253. DOI: 10.1002/(Sici)1521-3757(19991018)111:20<3250::Aid-Ange3250>3.0.Co;2-V |
0.444 |
|
1999 |
Gravel MC, Zhang C, Dinderman M, Laine RM. Octa(3-chloroammoniumpropyl) octasilsesquioxane Applied Organometallic Chemistry. 13: 329-336. DOI: 10.1002/(Sici)1099-0739(199904)13:4<329::Aid-Aoc870>3.0.Co;2-V |
0.325 |
|
1997 |
Déziel R, Malenfant E, Thibault C, Fréchette S, Gravel M. 2,6-bis[(2S)-tetrahydrofuran-2-yl]phenyl diselenide: An effective reagent for asymmetric electrophilic addition reactions to olefins Tetrahedron Letters. 38: 4753-4756. DOI: 10.1016/S0040-4039(97)01030-7 |
0.575 |
|
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