| Year |
Citation |
Score |
| 2019 |
Spino C, Aubert-Nicol S, Heinrich N, Lessard J. [Bis(trifluoroacetoxy)iodo]p-nitrobenzene and [Bis(trifluoroacetoxy)iodo]pentafluorobenzene as Lead Reagents for the Direct Ring Contraction of Lactams to Pyrrolidines Heterocycles. 99: 484. DOI: 10.3987/Com-18-S(F)43 |
0.394 |
|
| 2018 |
Croisetière JP, Spino C. O-Heterocycles from Unsaturated Carbonyls and Dimethoxycarbene. The Journal of Organic Chemistry. PMID 29682963 DOI: 10.1021/Acs.Joc.8B00613 |
0.314 |
|
| 2018 |
Aubert-Nicol S, Lessard J, Spino C. A Photorearrangement To Construct the ABDE Tetracyclic Core of Palau'amine. Organic Letters. PMID 29667828 DOI: 10.1021/Acs.Orglett.8B00819 |
0.404 |
|
| 2018 |
Gund M, Déry M, Spino C. Synthesis of carotol using a formal (4+1)-cycloaddition of chiral dialkoxycarbenes Canadian Journal of Chemistry. 96: 311-327. DOI: 10.1139/Cjc-2017-0594 |
0.45 |
|
| 2016 |
Gund M, Déry M, Amzallag V, Spino C. Dialkoxycarbenes in (4 + 1) Cycloadditions: Application to the Synthesis of Carotol. Organic Letters. PMID 27540758 DOI: 10.1021/Acs.Orglett.6B02023 |
0.475 |
|
| 2015 |
Déry M, Assouvie K, Heinrich N, Rajotte I, Lefebvre LP, Legault MA, Spino C. N-Heterocycles from chromium aminocarbenes. Organic Letters. 17: 1312-5. PMID 25702700 DOI: 10.1021/Acs.Orglett.5B00313 |
0.392 |
|
| 2014 |
Spino C. Modern Methods in Stereoselective Aldol Reactions. Edited by Rainer Mahrwald. Angewandte Chemie International Edition. 53: 5498-5498. DOI: 10.1002/Anie.201400982 |
0.355 |
|
| 2014 |
Spino C. Modern Methods in Stereoselective Aldol Reactions. Herausgegeben von Rainer Mahrwald. Angewandte Chemie. 126: 5602-5603. DOI: 10.1002/Ange.201400982 |
0.356 |
|
| 2013 |
Pichette S, Winter DK, Lessard J, Spino C. Converting cycloalkanones into N-heterocycles: formal synthesis of (-)-gephyrotoxin 287C. The Journal of Organic Chemistry. 78: 12532-44. PMID 24188015 DOI: 10.1021/Jo402217E |
0.766 |
|
| 2013 |
Déry M, Lefebvre LP, Aissa K, Spino C. N-Heteropolycyclic compounds from the formal intramolecular (4 + 1)-cycloaddition of chromium aminocarbenes. Organic Letters. 15: 5456-9. PMID 24117372 DOI: 10.1021/Ol4025887 |
0.412 |
|
| 2012 |
Pichette S, Aubert-Nicol S, Lessard J, Spino C. Photochemical and thermal ring-contraction of cyclic hydroxamic acid derivatives. The Journal of Organic Chemistry. 77: 11216-26. PMID 23198744 DOI: 10.1021/Jo3023507 |
0.769 |
|
| 2012 |
Beaumier F, Dupuis M, Spino C, Legault CY. Formal intramolecular (4 + 1)-cycloaddition of dialkoxycarbenes: control of the stereoselectivity and a mechanistic portrait. Journal of the American Chemical Society. 134: 5938-53. PMID 22404454 DOI: 10.1021/Ja211927B |
0.776 |
|
| 2012 |
Pichette S, Aubert-Nicol S, Lessard J, Spino C. Photochemical and thermal ring-contraction of cyclic hydroxamic acid derivatives Journal of Organic Chemistry. 77: 11216-11226. DOI: 10.1021/jo3023507 |
0.73 |
|
| 2012 |
Beaumier F, Dupuis M, Spino C, Legault CY. Formal intramolecular (4 + 1)-cycloaddition of dialkoxycarbenes: Control of the stereoselectivity and a mechanistic portrait Journal of the American Chemical Society. 134: 5938-5953. DOI: 10.1021/ja211927b |
0.757 |
|
| 2012 |
Pichette S, Aubert-Nicol S, Lessard J, Spino C. Regioselective photochemical rearrangement of N-mesyloxylactams European Journal of Organic Chemistry. 1328-1335. DOI: 10.1002/Ejoc.201101222 |
0.727 |
|
| 2011 |
Spino C. Menthone and p-menthyl-3-carboxaldehyde as chiral auxiliaries. Chemical Communications (Cambridge, England). 47: 4872-83. PMID 21387050 DOI: 10.1039/C0Cc05543C |
0.434 |
|
| 2011 |
Drouin A, Winter DK, Pichette S, Aubert-Nicol S, Lessard J, Spino C. Photochemical rearrangement of N-mesyloxylactams: stereospecific formation of N-heterocycles. The Journal of Organic Chemistry. 76: 164-9. PMID 21128634 DOI: 10.1021/Jo101805Q |
0.769 |
|
| 2011 |
Spino C. Copper-Mediated Asymmetric Allylic Alkylations Patai's Chemistry of Functional Groups. DOI: 10.1002/9780470682531.Pat0446 |
0.389 |
|
| 2010 |
Winter DK, Drouin A, Lessard J, Spino C. Photochemical rearrangement of N-chlorolactams: a route to N-heterocycles through concerted ring contraction. The Journal of Organic Chemistry. 75: 2610-8. PMID 20230016 DOI: 10.1021/Jo100181H |
0.411 |
|
| 2010 |
SPINO C, MAYES N, DESFOSSES H, SOTHEESWARAN S. ChemInform Abstract: Enantioselective Synthesis of (+)- and (-)-Dihydrokawain. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199652267 |
0.329 |
|
| 2010 |
LAVALLEE J, SPINO C, RUEL R, HOGAN KT, DESLONGCHAMPS P. ChemInform Abstract: Stereoselective Synthesis of cis-Decalins via Diels-Alder and Double Michael Addition of Substituted Nazarov Reagents. Cheminform. 24: no-no. DOI: 10.1002/chin.199305158 |
0.313 |
|
| 2009 |
Gagnon D, Spino C. Stereoselective synthesis of (+)-aspidofractinine Journal of Organic Chemistry. 74: 6035-6041. PMID 19603751 DOI: 10.1021/Jo9009497 |
0.476 |
|
| 2009 |
Arbour M, Roy S, Godbout C, Spino C. Stereoselective synthesis of (+)-euphococcinine and (-)-adaline Journal of Organic Chemistry. 74: 3806-3814. PMID 19371091 DOI: 10.1021/Jo9001992 |
0.445 |
|
| 2008 |
Perreault S, Poirier M, Léveillé P, René O, Joly P, Dory Y, Spino C. Mechanism and regioselectivity of the cycloaddition of thiones derived from Meldrum's acid, malonates, or other dicarbonyls. The Journal of Organic Chemistry. 73: 7457-66. PMID 18771325 DOI: 10.1021/Jo800945Y |
0.364 |
|
| 2008 |
Lauzon S, Tremblay F, Gagnon D, Godbout C, Chabot C, Mercier-Shanks C, Perreault S, DeSève H, Spino C. Sterically biased 3,3-sigmatropic rearrangement of chiral allylic azides: Application to the total syntheses of alkaloids Journal of Organic Chemistry. 73: 6239-6250. PMID 18642871 DOI: 10.1021/Jo800817P |
0.491 |
|
| 2008 |
Lauzon S, Tremblay F, Gagnon D, Godbout C, Chabot C, Mercier-Shanks C, Perreault S, DeSeve H, Spino C. ChemInform Abstract: Sterically Biased 3,3-Sigmatropic Rearrangement of Chiral Allylic Azides: Application to the Total Syntheses of Alkaloids. Cheminform. 39. DOI: 10.1002/chin.200852060 |
0.319 |
|
| 2007 |
Boisvert L, Beaumier F, Spino C. Evidence for a concerted [4 + 1]- cycloaddition between electron-rich carbenes and electron-deficient dienes. Organic Letters. 9: 5361-3. PMID 18027955 DOI: 10.1021/Ol702172T |
0.757 |
|
| 2007 |
Minville J, Girardin M, Spino C. Efficient preparation of chiral non-racemic sulfur compounds Canadian Journal of Chemistry. 85: 603-618. DOI: 10.1139/V07-091 |
0.424 |
|
| 2007 |
Boisvert L, Beaumier F, Spino C. Evidence for a concerted [4 + 1]-cycloaddition between electron-rich carbenes and electron-deficient dienes Organic Letters. 9: 5361-5363. DOI: 10.1021/ol702172t |
0.736 |
|
| 2007 |
Spino C, Boisvert L, Douville J, Roy S, Lauzon S, Minville J, Gagnon D, Beaumier F, Chabot C. Cleavage of a Chiral Auxiliary Using RCM on an Especially Sterically Crowded Alkene: Syntheses of Chiral Carbo- and Heterocycles. Cheminform. 38. DOI: 10.1002/chin.200720044 |
0.324 |
|
| 2006 |
Perreault S, Spino C. Meldrum's acid-derived thione dienophile in a convergent and stereoselective synthesis of a tetracyclic quassinoid intermediate Organic Letters. 8: 4385-4388. PMID 16986906 DOI: 10.1021/Ol060892T |
0.459 |
|
| 2006 |
Roy S, Spino C. Stereocontrolled formation of amino acids and N-heterocycles bearing a quaternary chiral carbon Organic Letters. 8: 939-942. PMID 16494479 DOI: 10.1021/Ol053061G |
0.377 |
|
| 2006 |
Boisvert L, Beaumier F, Spino C. A chiral auxiliary cleavable by ring-closing alkene metathesis - Efficient synthesis of chiral nonracemic cycloalkenes Canadian Journal of Chemistry. 84: 1290-1293. DOI: 10.1139/V06-095 |
0.791 |
|
| 2006 |
Spino C, Boisvert L, Douville J, Roy S, Lauzon S, Minville J, Gagnon D, Beaumier F, Chabot C. Cleavage of a chiral auxiliary using RCM on an especially sterically crowded alkene: Syntheses of chiral carbo- and heterocycles Journal of Organometallic Chemistry. 691: 5336-5355. DOI: 10.1016/J.Jorganchem.2006.07.028 |
0.762 |
|
| 2005 |
Dion A, Dubé P, Spino C. A triple diene-transmissive Diels-Alder strategy to build the quassinoid framework Organic Letters. 7: 5601-5604. PMID 16321001 DOI: 10.1021/Ol0522236 |
0.442 |
|
| 2005 |
Gagnon D, Lauzon S, Godbout C, Spino C. Sterically biased 3,3-sigmatropic rearrangement of azides: efficient preparation of nonracemic alpha-amino acids and heterocycles. Organic Letters. 7: 4769-71. PMID 16209531 DOI: 10.1021/Ol052034N |
0.376 |
|
| 2005 |
Spino C, Gund VG, Nadeau C. A chiral cyclohexanone linked to polystyrene for solid-phase synthesis of chiral α-carbonyls Journal of Combinatorial Chemistry. 7: 345-352. PMID 15762765 DOI: 10.1021/Cc049859T |
0.389 |
|
| 2004 |
Spino C, Godbout C, Beaulieu C, Harter M, Mwene-Mbeja TM, Boisvert L. p-Menthane-3-carboxaldehyde: a useful chiral auxiliary for the synthesis of chiral quaternary carbons of high enantiomeric purity. Journal of the American Chemical Society. 126: 13312-9. PMID 15479086 DOI: 10.1021/Ja046084J |
0.433 |
|
| 2004 |
Spino C, Rezaei H, Dupont-Gaudet K, Bélanger F. Inter- and intramolecular [4 + 1]-cycloadditions between electron-poor dienes and electron-rich carbenes. Journal of the American Chemical Society. 126: 9926-7. PMID 15303859 DOI: 10.1021/Ja046344X |
0.405 |
|
| 2004 |
Spino C, Tremblay MC, Gobdout C. A stereodivergent approach to amino acids, amino alcohols, or oxazolidinones of high enantiomeric purity Organic Letters. 6: 2801-2804. PMID 15281773 DOI: 10.1021/Ol048936Q |
0.303 |
|
| 2004 |
Spino C, Rezaei H, Dory YL. Characteristics of the two frontier orbital interactions in the Diels-Alder cycloaddition. The Journal of Organic Chemistry. 69: 757-64. PMID 14750802 DOI: 10.1021/Jo0353740 |
0.351 |
|
| 2004 |
Spino C, Allan M. An iterative approach to three fragments of ionomycin Canadian Journal of Chemistry. 82: 177-184. DOI: 10.1139/V03-182 |
0.382 |
|
| 2003 |
Spino C, Gobdout C. A stereodivergent approach to chiral nonracemic N-protected α,α-dialkylated amino acids Journal of the American Chemical Society. 125: 12106-12107. PMID 14518992 DOI: 10.1021/Ja037078A |
0.35 |
|
| 2003 |
Spino C, Hill B, Dubé P, Gingras S. A diene-transmissive approach to the quassinoid skeleton Canadian Journal of Chemistry. 81: 81-108. DOI: 10.1139/V02-196 |
0.326 |
|
| 2003 |
Spino C. Chiral enolate equivalents. A review Organic Preparations and Procedures International. 35: 1-140. DOI: 10.1080/00304940309355794 |
0.335 |
|
| 2002 |
Spino C, Granger MC, Tremblay MC. Increased Felkin-Anh selectivity using AlMe(3) in the addition of vinyllithiums to alpha-chiral aldehydes: do "ate" complexes play any role? Organic Letters. 4: 4735-7. PMID 12489974 DOI: 10.1021/Ol027236N |
0.333 |
|
| 2002 |
Spino C, Granger MC, Boisvert L, Beaulieu C. Increased Felkin-Anh selectivity in nucleophilic additions to α-chiral aldehydes using vinylalanes Tetrahedron Letters. 43: 4183-4185. DOI: 10.1016/S0040-4039(02)00753-0 |
0.408 |
|
| 2000 |
Spino C, Beaulieu C, Lafreniere J. Chiral alpha-substituted carbonyls and alcohols from the S(N)2' displacement of cuprates on chiral carbonates: An alternative to the alkylation of chiral enolates The Journal of Organic Chemistry. 65: 7091-7. PMID 11031033 DOI: 10.1021/Jo000810T |
0.448 |
|
| 2000 |
Spino C, Beaulieu C. A Novel Method To Generate Chiral Quaternary Carbon Centers of High Enantiomeric Purity Using a Highly Stereoselective Addition of Vinylalanes to a Chiral Aldehyde We acknowledge the Natural Sciences and Engineering Council of Canada and Merck-Frosst for financial support. Angewandte Chemie (International Ed. in English). 39: 1930-1932. PMID 10940984 DOI: 10.1002/1521-3773(20000602)39:11<1930::Aid-Anie1930>3.0.Co;2-J |
0.384 |
|
| 2000 |
Spino C, Frechette S. Synthesis of non-racemic unsymmetrical tetrasubstituted vinylallenes Tetrahedron Letters. 41: 8033-8036. DOI: 10.1016/S0040-4039(00)01406-4 |
0.448 |
|
| 1999 |
Spino C, Barriault N. Radical cyclization of polyenes initiated by attack of trialkyltin or germanium radical on an ynone Journal of Organic Chemistry. 64: 5292-5298. DOI: 10.1021/Jo9905524 |
0.34 |
|
| 1999 |
Beaulieu C, Spino C. Efficient syntheses of optically active 2-arylalkanoic acids Tetrahedron Letters. 40: 1637-1640. DOI: 10.1016/S0040-4039(99)00055-6 |
0.4 |
|
| 1998 |
Spino C, Crawford J, Cui Y, Gugelchuk M. The dimerisation of 2-methoxycarbonylbuta-1,3-diene: the importance of paralocalisation energy in assessing diene reactivity Journal of the Chemical Society-Perkin Transactions 1. 1499-1506. DOI: 10.1039/A708199E |
0.314 |
|
| 1998 |
Spino C, Thibault C, Gingras S. Stereoselective Construction of Tetrasubstituted Exocyclic Alkenes from the [4 + 2]-Cycloaddition of Vinylallenes The Journal of Organic Chemistry. 63: 5283-5287. DOI: 10.1021/Jo980482L |
0.405 |
|
| 1998 |
Spino C, Pesant M, Dory Y. Neues vom Diels-Alder-Übergangszustand Angewandte Chemie. 110: 3454-3457. DOI: 10.1002/(Sici)1521-3757(19981204)110:23<3454::Aid-Ange3454>3.0.Co;2-5 |
0.302 |
|
| 1997 |
Spino C, Clouston LL, Berg DJ. Lanthanide catalysts for the hetero Diels-Alder reaction: Effect of ligand structure and acidity Canadian Journal of Chemistry. 75: 1047-1054. DOI: 10.1139/V97-125 |
0.327 |
|
| 1996 |
Spino C, Clouston L, Berg D. Novel, air-stable, lanthanide catalysts for the hetero Diels-Alder reaction Canadian Journal of Chemistry. 74: 1762-1764. DOI: 10.1139/V96-195 |
0.307 |
|
| 1996 |
Spino C, Mayes N, Desfossés H. Enantioselective synthesis of (+)- and (-)-dihydrokawain Tetrahedron Letters. 37: 6503-6506. DOI: 10.1016/0040-4039(96)01429-3 |
0.361 |
|
| 1995 |
Spino C, Crawford J, Bishop J. Sequential Diels-Alder Reactions on a 1,3,7,9-Tetraene: An Efficient and Stereoselective Route to the Perhydrophenanthrene Skeleton Journal of Organic Chemistry. 60: 844-851. DOI: 10.1021/Jo00109A014 |
0.4 |
|
| 1995 |
Spino C, Lal J, Sotheeswaran S, Aalbersberg W. Three prenylated phenolic benzophenones from Garcinia myrtifolia Phytochemistry. 38: 233-236. DOI: 10.1016/0031-9422(94)00589-L |
0.315 |
|
| 1994 |
Spino C, Liu G, Tu N, Girard S. The diene - transmissive [4 + 2]-cycloaddition strategy: Stereoselective synthesis of advanced intermediates to quassinoids Journal of Organic Chemistry. 59: 5596-5608. DOI: 10.1021/Jo00098A017 |
0.421 |
|
| 1994 |
Spino C, Crawford J. An expedient and stereoselective route to the perhydrophenanthrene skeleton via sequential Diels-Alder reactions Tetrahedron Letters. 35: 5559-5562. DOI: 10.1016/S0040-4039(00)77246-7 |
0.473 |
|
| 1994 |
Spino C, Tu N. Enantioselective synthesis of an advanced intermediate to quassinoids Tetrahedron Letters. 35: 3683-3686. DOI: 10.1016/S0040-4039(00)73071-1 |
0.379 |
|
| 1993 |
Alderdice M, Spino C, Weiler L. The synthesis of the isomeric components of San Jose scale pheromone - An illustration of a stereospecific synthesis of trisubstituted alkenes Canadian Journal of Chemistry. 71: 1955-1963. DOI: 10.1139/V93-242 |
0.689 |
|
| 1993 |
Spino C, Crawford J. 2-Carbomethoxy-1,3-butadiene: an electronically activated diene in [4 + 2] cycloadditions with electron-deficient dienophiles Canadian Journal of Chemistry. 71: 1094-1097. DOI: 10.1139/V93-145 |
0.392 |
|
| 1993 |
Spino C, Liu G. A stereoselective diene-transmissive [4 + 2]-cycloaddition strategy for the construction of the tetracyclic quassinoid framework Journal of Organic Chemistry. 58: 817-819. DOI: 10.1021/Jo00056A008 |
0.42 |
|
| 1992 |
Lavallée J, Spino C, Ruel R, Hogan KT, Deslongchamps P. Stereoselective synthesis of cis-decalins via Diels–Alder and double Michael addition of substituted Nazarov reagents Canadian Journal of Chemistry. 70: 1406-1426. DOI: 10.1139/V92-179 |
0.357 |
|
| 1990 |
Spino C, Deslongchamps P. Highly stereoselective double michael cyclization of 1-phenylsulfinyl and sulfonyl analogues of the nazarov reagent Tetrahedron Letters. 31: 3969-3972. DOI: 10.1016/S0040-4039(00)94474-5 |
0.432 |
|
| 1987 |
Spino C, Weiler L. A stereoselective synthesis of the tetrahydrofuran unit in ionomycin Tetrahedron Letters. 28: 731-734. DOI: 10.1016/S0040-4039(01)80974-6 |
0.638 |
|
| 1984 |
Alderdice M, Spino C, Weiler L. Synthesis of the three isomeric components of San Jose scale pheromone Tetrahedron Letters. 25: 1643-1646. DOI: 10.1016/S0040-4039(01)81133-3 |
0.607 |
|
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