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Volumn 66, Issue 38, 2010, Pages 7618-7624
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An efficient synthesis of chiral isoquinuclidines by Diels - Alder reaction using Lewis acid catalyst
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Author keywords
1,2 Dihydropyridine; Alkaloid; Diastereoselectivity; Diels Alder reaction; Isoquinuclidine; Lewis acid catalyst
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Indexed keywords
1 METHOXYCARBONYL 1,2 DIHYDROPYRIDINE;
1 PHENOXYCARBONYL 1,2 DIHYDROPYRIDINE;
2 METHOXYCARBONYL 2 AZABICYCLO[2.2.2]OCT 5 ENE 7 METHYL CARBOXYLATE;
7 (2,10 CAMPHORSULTAM 4' CARBONYL) 2 AZA BICYCLO[2.2.2]OCT 5 ENE CARBOXYLIC ACID METHYL ESTER;
7 (2,10 CAMPHORSULTAM 4' CARBONYL) 2 AZA BICYCLO[2.2.2]OCT 5 ENE CARBOXYLIC ACID PHENYL ESTER;
HAFNIUM TETRACHLORIDE;
LEWIS ACID;
N ACRYLOYL 2,10 CAMPHORSULTAM;
QUINUCLIDINE DERIVATIVE;
TITANIUM TETRACHLORIDE;
UNCLASSIFIED DRUG;
ZIRCONIUM TETRACHLORIDE;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CATALYST;
CYCLOADDITION;
DIELS ALDER REACTION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEREOCHEMISTRY;
ALNUS;
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EID: 77956173859
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2010.07.026 Document Type: Article |
Times cited : (26)
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References (23)
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