| Year |
Citation |
Score |
| 2023 |
Tran H, McGee P, Barriault L. Formal Synthesis of Salvinorin A via Gold Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301640. PMID 37310277 DOI: 10.1002/chem.202301640 |
0.454 |
|
| 2022 |
Hébert M, Bellavance G, Barriault L. Total Synthesis of Ginkgolide C and Formal Syntheses of Ginkgolides A and B. Journal of the American Chemical Society. 144: 17792-17796. PMID 36150149 DOI: 10.1021/jacs.2c08351 |
0.345 |
|
| 2021 |
Barriault L, Tran H, Revol G, Poyser A. Divergent and Modular Synthesis of Terpenoid Scaffolds via a Au(I) Catalyzed One-Pot Cascade. Angewandte Chemie (International Ed. in English). PMID 34714952 DOI: 10.1002/anie.202110575 |
0.414 |
|
| 2020 |
Zidan M, McCallum T, Swann R, Barriault L. Formal Bromine Atom Transfer Radical Addition of Nonactivated Bromoalkanes Using Photoredox Gold Catalysis. Organic Letters. PMID 33040532 DOI: 10.1021/acs.orglett.0c03030 |
0.362 |
|
| 2020 |
Rohe S, Révol G, Marmin T, Barriault D, Barriault L. Single-Electron Transfer from Dimsyl Anion in the Alkylation of Phenols. The Journal of Organic Chemistry. PMID 31913644 DOI: 10.1021/Acs.Joc.9B03237 |
0.386 |
|
| 2019 |
Brousseau J, Xolin A, Barriault L. A Nine-Step Formal Synthesis of (±)-Morphine. Organic Letters. 21: 1347-1349. PMID 30785291 DOI: 10.1021/Acs.Orglett.9B00044 |
0.383 |
|
| 2018 |
Barriault L, McCallum T, Rohe S, Morris A. HAT Reactions Via Photoredox Catalyzed Chlorine Atom Generation. Angewandte Chemie (International Ed. in English). PMID 30295981 DOI: 10.1002/Anie.201810187 |
0.4 |
|
| 2018 |
Rohe S, McCallum T, Morris AO, Barriault L. Transformations of Isonitriles with Bromoalkanes using Photoredox Gold Catalysis. The Journal of Organic Chemistry. PMID 29979602 DOI: 10.1021/Acs.Joc.8B01380 |
0.461 |
|
| 2018 |
Bellavance G, Barriault L. Modular Total Syntheses of Hyperforin, Papuaforins A, B and C via Gold(I)-Catalyzed Carbocyclization. The Journal of Organic Chemistry. PMID 29732886 DOI: 10.1021/Acs.Joc.8B00426 |
0.468 |
|
| 2018 |
Zidan M, Rohe S, McCallum T, Barriault L. Recent advances in mono and binuclear gold photoredox catalysis Catalysis Science & Technology. 8: 6019-6028. DOI: 10.1039/C8Cy01765D |
0.345 |
|
| 2018 |
Rohe S, Morris AO, McCallum T, Barriault L. Frontispiece: Hydrogen Atom Transfer Reactions via Photoredox Catalyzed Chlorine Atom Generation Angewandte Chemie International Edition. 57. DOI: 10.1002/Anie.201884861 |
0.319 |
|
| 2017 |
McCallum T, Pitre SP, Morin M, Scaiano JC, Barriault L. The photochemical alkylation and reduction of heteroarenes. Chemical Science. 8: 7412-7418. PMID 29163892 DOI: 10.1039/C7Sc03768F |
0.374 |
|
| 2017 |
McGee P, Bétournay G, Barabé F, Barriault L. A 11-Steps Total Synthesis of Magellanine through a Gold(I)-Catalyzed Dehydro Diels-Alder Reaction. Angewandte Chemie (International Ed. in English). PMID 28079949 DOI: 10.1002/Anie.201611606 |
0.563 |
|
| 2017 |
Zidan M, McCallum T, Thai-Savard L, Barriault L. Photoredox meets gold Lewis acid catalysis in the alkylative semipinacol rearrangement: a photocatalyst with a dark side Organic Chemistry Frontiers. 4: 2092-2096. DOI: 10.1039/C7Qo00590C |
0.388 |
|
| 2017 |
McGee P, Brousseau J, Barriault L. Development of New Gold (I)-Catalyzed Carbocyclizations and their Applications in the Synthesis of Natural Products Israel Journal of Chemistry. 58: 511-520. DOI: 10.1002/Ijch.201700054 |
0.434 |
|
| 2016 |
Tran H, McCallum T, Morin M, Barriault L. Homocoupling of Iodoarenes and Bromoalkanes Using Photoredox Gold Catalysis: A Light Enabled Au(III) Reductive Elimination. Organic Letters. PMID 27522864 DOI: 10.1021/Acs.Orglett.6B02021 |
0.428 |
|
| 2016 |
Cannillo A, Schwantje TR, Bégin M, Barabé F, Barriault L. Gold-Catalyzed Photoredox C(sp(2)) Cyclization: Formal Synthesis of (±)-Triptolide. Organic Letters. PMID 27177198 DOI: 10.1021/Acs.Orglett.6B00968 |
0.463 |
|
| 2016 |
Barriault L, McCallum T, Rohe S. Thieme Chemistry Journals Awardees – Where Are They Now? What’s Golden: Recent Advances in Organic Transformations Using Photoredox Gold Catalysis Synlett. 28: 289-305. DOI: 10.1055/S-0036-1588644 |
0.406 |
|
| 2016 |
McCallum T, Jouanno LA, Cannillo A, Barriault L. Persulfate-Enabled Direct C-H Alkylation of Heteroarenes with Unactivated Ethers Synlett. 27: 1282-1286. DOI: 10.1055/S-0035-1561338 |
0.423 |
|
| 2016 |
McCallum T, Barriault L. Direct alkylation of heteroarenes with unactivated bromoalkanes using photoredox gold catalysis Chemical Science. 7: 4754-4758. DOI: 10.1039/C6Sc00807K |
0.463 |
|
| 2015 |
McGee P, Bellavance G, Korobkov I, Tarasewicz A, Barriault L. Synthesis and Isolation of Organogold Complexes through a Controlled 1,2-Silyl Migration. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 9662-5. PMID 26037504 DOI: 10.1002/Chem.201501648 |
0.416 |
|
| 2015 |
Kaldas SJ, Cannillo A, McCallum T, Barriault L. Indole Functionalization via Photoredox Gold Catalysis. Organic Letters. 17: 2864-6. PMID 25997468 DOI: 10.1021/Acs.Orglett.5B01260 |
0.402 |
|
| 2015 |
McCallum T, Barriault L. Light-enabled synthesis of anhydrides and amides. The Journal of Organic Chemistry. 80: 2874-8. PMID 25689228 DOI: 10.1021/Acs.Joc.5B00003 |
0.451 |
|
| 2015 |
McTiernan CD, Morin M, McCallum T, Scaiano JC, Barriault L. Polynuclear gold(i) complexes in photoredox catalysis: Understanding their reactivity through characterization and kinetic analysis Catalysis Science and Technology. 6: 201-207. DOI: 10.1039/C5Cy01259G |
0.395 |
|
| 2015 |
McCallum T, Slavko E, Morin M, Barriault L. Light-mediated deoxygenation of alcohols with a dimeric gold catalyst European Journal of Organic Chemistry. 2015: 81-85. DOI: 10.1002/Ejoc.201403351 |
0.338 |
|
| 2014 |
Bellavance G, Barriault L. Total syntheses of hyperforin and papuaforins A-C, and formal synthesis of nemorosone through a gold(I)-catalyzed carbocyclization. Angewandte Chemie (International Ed. in English). 53: 6701-4. PMID 24838522 DOI: 10.1002/Anie.201403939 |
0.535 |
|
| 2014 |
Barriault L, Sow B, Sherburn MS. Consecutive Sigmatropic Rearrangements Comprehensive Organic Synthesis: Second Edition. 5: 978-998. DOI: 10.1016/B978-0-08-097742-3.00522-X |
0.694 |
|
| 2013 |
Morin M, Levesque P, Barriault L. Gold(I)-catalyzed domino cyclization for the synthesis of polyaromatic heterocycles. Beilstein Journal of Organic Chemistry. 9: 2625-8. PMID 24367426 DOI: 10.3762/Bjoc.9.297 |
0.509 |
|
| 2013 |
Barabé F, Levesque P, Sow B, Bellavance G, Bétournay G, Barriault L. Gold(I)-catalyzed formation of bridged and fused carbocycles Pure and Applied Chemistry. 85: 1161-1173. DOI: 10.1351/Pac-Con-13-01-02 |
0.71 |
|
| 2012 |
Poulin J, Grisé-Bard CM, Barriault L. A formal synthesis of vinigrol. Angewandte Chemie (International Ed. in English). 51: 2111-4. PMID 22259041 DOI: 10.1002/Anie.201108779 |
0.679 |
|
| 2012 |
Barriault L, Denissova I, Goulet N. Mechanistic investigation of the domino oxy-cope/ene/claisen reaction and its application to the synthesis of desdimethyl ambliol B Synthesis (Germany). 44: 1833-1840. DOI: 10.1055/S-0031-1291144 |
0.511 |
|
| 2012 |
Barriault L, Poulin J. 2.20 Selected Diastereoselective Reactions: Ionic and Zwitterionic Cyclizations Comprehensive Chirality. 2: 607-624. DOI: 10.1016/B978-0-08-095167-6.00211-1 |
0.693 |
|
| 2011 |
Barabé F, Levesque P, Korobkov I, Barriault L. Synthesis of fused carbocycles via a selective 6-endo dig gold(I)-catalyzed carbocyclization. Organic Letters. 13: 5580-3. PMID 21916520 DOI: 10.1021/Ol202314Q |
0.474 |
|
| 2011 |
Sow B, Bellavance G, Barabé F, Barriault L. One-pot Diels-Alder cycloaddition/gold(I)-catalyzed 6-endo-dig cyclization for the synthesis of the complex bicyclo[3.3.1]alkenone framework. Beilstein Journal of Organic Chemistry. 7: 1007-13. PMID 21915201 DOI: 10.3762/Bjoc.7.114 |
0.76 |
|
| 2010 |
Hooper J, Sauer EL, Arns S, Woo TK, Barriault L. On the origin of altered diastereomeric ratios for anionic versus neutral reaction conditions in the oxy-Cope/ene reaction: an interplay of experiment and computational modeling. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 14124-30. PMID 20957622 DOI: 10.1002/Chem.201001302 |
0.394 |
|
| 2010 |
Beingessner RL, Farand JA, Barriault L. Progress toward the total synthesis of (±)-havellockate. The Journal of Organic Chemistry. 75: 6337-46. PMID 20815361 DOI: 10.1021/Jo101279Z |
0.467 |
|
| 2010 |
Barabe F, Betournay G, Bellavance G, Barriault L. ChemInform Abstract: Gold-Catalyzed Synthesis of Carbon-Bridged Medium-Sized Rings Cheminform. 41. DOI: 10.1002/CHIN.201004053 |
0.316 |
|
| 2010 |
BARRIAULT L, DESLONGCHAMPS P. ChemInform Abstract: Synthesis of 17-Membered Ring Macrocycle: Studies Toward the Enantioselective Synthesis of Fusidic Acid. Cheminform. 29: no-no. DOI: 10.1002/chin.199835282 |
0.566 |
|
| 2010 |
BARRIAULT L, OUELLET SG, DESLONGCHAMPS P. ChemInform Abstract: Transannular Diels-Alder Reaction Studies with an Activated Dienophile. An Enantioselective Synthesis of an A.B.C.[6.6.6.] trans-syn-cis Tricycle. Cheminform. 29: no-no. DOI: 10.1002/chin.199807032 |
0.377 |
|
| 2009 |
Poulin J, Grisé-Bard CM, Barriault L. Pericyclic domino reactions: concise approaches to natural carbocyclic frameworks. Chemical Society Reviews. 38: 3092-101. PMID 19847344 DOI: 10.1039/B819798A |
0.709 |
|
| 2009 |
Barabé F, Bétournay G, Bellavance G, Barriault L. Gold-catalyzed synthesis of carbon-bridged medium-sized rings. Organic Letters. 11: 4236-8. PMID 19739690 DOI: 10.1021/Ol901722Q |
0.419 |
|
| 2008 |
Riou M, Barriault L. De novo synthesis of (+)-isofregenedol. The Journal of Organic Chemistry. 73: 7436-9. PMID 18698826 DOI: 10.1021/Jo801365Z |
0.463 |
|
| 2008 |
Clément R, Grisé CM, Barriault L. Stereocontrolled synthesis of carbocycles via four successive pericyclic reactions. Chemical Communications (Cambridge, England). 3004-6. PMID 18688329 DOI: 10.1039/B803898H |
0.517 |
|
| 2008 |
Grisé CM, Rodrigue EM, Barriault L. Gold(I)-catalyzed benzannulation of 3-hydroxy-1,5-enynes: an efficient synthesis of substituted tetrahydronaphthalenes and related compounds Tetrahedron. 64: 797-808. DOI: 10.1016/J.Tet.2007.10.084 |
0.525 |
|
| 2007 |
Arns S, Lebrun ME, Grisé CM, Denissova I, Barriault L. Diastereoselective construction of quaternary carbons directed via macrocyclic ring conformation: formal synthesis of (-)-mesembrine. The Journal of Organic Chemistry. 72: 9314-22. PMID 17958376 DOI: 10.1021/Jo701833V |
0.444 |
|
| 2007 |
Arns S, Barriault L. Cascading pericyclic reactions: building complex carbon frameworks for natural product synthesis. Chemical Communications (Cambridge, England). 2211-21. PMID 17534496 DOI: 10.1039/B700054P |
0.514 |
|
| 2007 |
Grisé CM, Tessier G, Barriault L. Synthesis of the tricyclic core of vinigrol via an intramolecular Diels-Alder reaction. Organic Letters. 9: 1545-8. PMID 17362025 DOI: 10.1021/Ol0702977 |
0.537 |
|
| 2007 |
Sauer ELO, Hooper J, Woo T, Barriault L. Origin of diastereoselectivity in the tandem oxy-Cope/Claisen/ene reaction: Experimental and theoretical studies of the ring inversion mechanism Journal of the American Chemical Society. 129: 2112-2119. PMID 17256936 DOI: 10.1021/Ja066830F |
0.432 |
|
| 2006 |
Grisé CM, Barriault L. Gold-catalyzed synthesis of substituted tetrahydronaphthalenes. Organic Letters. 8: 5905-8. PMID 17134302 DOI: 10.1021/Ol062582G |
0.546 |
|
| 2006 |
Arns S, Barriault L. Concise synthesis of the neo-clerodane skeleton of teucrolivin A using a pericyclic reaction cascade. The Journal of Organic Chemistry. 71: 1809-16. PMID 16496965 DOI: 10.1021/Jo052052I |
0.544 |
|
| 2005 |
Lavigne RM, Riou M, Girardin M, Morency L, Barriault L. Synthesis of highly functionalized bicyclo[m.n.1]alkanones via a cationic reaction cascade. Organic Letters. 7: 5921-3. PMID 16354100 DOI: 10.1021/Ol0527072 |
0.477 |
|
| 2005 |
Morency L, Barriault L. Studies toward the total synthesis of vinigrol. synthesis of the octalin ring. The Journal of Organic Chemistry. 70: 8841-53. PMID 16238317 DOI: 10.1021/Jo051318I |
0.451 |
|
| 2005 |
Warrington JM, Barriault L. Synthesis of the C7-C15 trans decalin portion of the natural antibiotic tetrodecamycin. Organic Letters. 7: 4589-92. PMID 16209486 DOI: 10.1021/Ol051715F |
0.456 |
|
| 2005 |
Gauvreau D, Barriault L. Conservation of the planar chiral information in the tandem oxy-cope/ene reaction. The Journal of Organic Chemistry. 70: 1382-8. PMID 15704974 DOI: 10.1021/Jo047916Z |
0.497 |
|
| 2004 |
Sauer EL, Barriault L. Studies toward the total synthesis of Wiedemannic acid. Organic Letters. 6: 3329-32. PMID 15355044 DOI: 10.1021/Ol0487635 |
0.496 |
|
| 2004 |
Sauer EL, Barriault L. Highly efficient transfer of chirality from macrocyclic conformation in the tandem oxy-Cope/Claisen/ene reaction. Journal of the American Chemical Society. 126: 8569-75. PMID 15238016 DOI: 10.1021/Ja048301M |
0.517 |
|
| 2004 |
Barriault L, Ang PJ, Lavigne RM. Rapid assembly of the bicyclo[5.3.1]undecenone core of penostatin F: a successive Diels-Alder/Claisen reaction strategy with an efficient stereochemical relay. Organic Letters. 6: 1317-9. PMID 15070326 DOI: 10.1021/Ol049680R |
0.407 |
|
| 2004 |
Farand JA, Denissova I, Barriault L. Microwave assisted pericyclic reactions in cascade to construct decalin frameworks possessing quaternary centers. Scope and limitations Heterocycles. 62: 735-748. DOI: 10.3987/Com-03-S(P)72 |
0.535 |
|
| 2004 |
Morency L, Barriault L. Stereoselective synthesis of the cis-decalin subunit of vinigrol via three pericyclic reactions in cascade Tetrahedron Letters. 45: 6105-6107. DOI: 10.1016/J.Tetlet.2004.06.071 |
0.49 |
|
| 2003 |
Barriault L, Thomas JD, Clément R. Highly stereoselective hydroxy-directed Diels-Alder reaction. The Journal of Organic Chemistry. 68: 2317-23. PMID 12636397 DOI: 10.1021/Jo020664M |
0.452 |
|
| 2003 |
Denissova I, Barriault L. Stereoselective formation of quaternary carbon centers and related functions Tetrahedron. 59: 10105-10146. DOI: 10.1016/J.Tet.2003.10.039 |
0.302 |
|
| 2002 |
Barriault L, Denissova I. Highly diastereoselective synthesis of decalin skeletons with quaternary carbon centers via the tandem oxy-Cope/ene/Claisen reaction. Organic Letters. 4: 1371-4. PMID 11950365 DOI: 10.1021/ol025694q |
0.446 |
|
| 2001 |
Fortin S, Barriault L, Dory YL, Deslongchamps P. Theoretical and experimental determination of the effects governing the transannular Diels-Alder reaction of trans-trans-cis systems with or without activation of the dienophile. Journal of the American Chemical Society. 123: 8210-6. PMID 11516271 DOI: 10.1021/Ja0109491 |
0.676 |
|
| 2001 |
Barriault L, Deon DH. Total synthesis of (+)-arteanniun M using the tandem oxy-cope/ene reaction Organic Letters. 3: 1925-1927. PMID 11405746 DOI: 10.1021/ol015970l |
0.391 |
|
| 2000 |
Warrington JM, Yap GPA, Barriault L. Tandem oxy-Cope/transannular ene reaction of 1,2-divinylcyclohexanols Organic Letters. 2: 663-665. DOI: 10.1021/Ol005502W |
0.477 |
|
| 2000 |
Paquette LA, Barriault L, Pissarnitski D, Johnston JN. Stereocontrolled elaboration of natural (-)-polycavernoside A, a powerfully toxic metabolite of the red alga Polycavernosa tsudai Journal of the American Chemical Society. 122: 619-631. DOI: 10.1021/Ja993487O |
0.624 |
|
| 1999 |
Barriault L, Boulet SL, Fujiwara K, Murai A, Paquette LA, Yotsu-Yamashita M. Synthesis and biological evaluation of analogs of the marine toxin polycavernoside A. Bioorganic & Medicinal Chemistry Letters. 9: 2069-72. PMID 10450983 DOI: 10.1016/S0960-894X(99)00341-8 |
0.346 |
|
| 1999 |
Paquette LA, Barriault L, Pissarnitski D. A convergent total synthesis of the macrolactone disaccharide toxin (- )-polycavernoside A Journal of the American Chemical Society. 121: 4542-4543. DOI: 10.1021/Ja990384X |
0.507 |
|
| 1998 |
Paquette LA, Pissarnitski D, Barriault L. A Modular Enantioselective Approach to Construction of the Macrolactone Core of Polycavernoside A. The Journal of Organic Chemistry. 63: 7389-7398. PMID 11672388 DOI: 10.1021/Jo981083T |
0.542 |
|
| 1997 |
Barriault L, Quellet SG, Deslongchamps P. Transannular Diels-Alder reaction studies with an activated dienophile. An enantioselective synthesis of an A.B.C.[6.6.6.] trans-syn-cis tricycle Tetrahedron. 53: 14937-14956. DOI: 10.1016/S0040-4020(97)00997-6 |
0.586 |
|
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