Stereospecific synthesis of trans -5,6-dihydropyridinones

Synthesis

Volumn , Issue 5, 2011, Pages 759-763

  Chou, Shang Shing P ^a   Yang, Tsung Han ^a   Wu, Wan Shiuan ^a   Chiu, Tzu Han ^a  

^a FU JEN CATHOLIC UNIVERSITY   (Taiwan)

Author keywords

aza Diels Alder reaction; epiquinamide; homopumiliotoxin 223G; trans 1 hydroxyquinolizidin 4 one; trans 5,6 dihydropyridi nones

Indexed keywords

DIELS-ALDER REACTION; EPIQUINAMIDE; HOMOPUMILIOTOXIN 223G; TRANS -1-HYDROXYQUINOLIZIDIN-4-ONE; TRANS -5,6-DIHYDROPYRIDI-NONES;

SYNTHESIS (CHEMICAL);

1 HYDROXYQUINOLIZIDIN 4 ONE; 5 BROMO 6 (4 CHLOROBUTYL) 4 (PHENYLTHIO) 1 TOSYL 5,6 DIHYDROPYRIDIN 2(1H) ONE; 5 BROMO 6 METHYL 4(PHENYLTHIO) 1 TOSYL 5,6 DIHYDROPYRIDIN 2(1H) ONE; 5,6 DIHYDROPYRIDINE DERIVATIVE; ALKALOID; BROMINE; CARBON; DIHYDROPYRIDINE DERIVATIVE; EPIQUINAMIDE; HOMOPUMILIOTOXIN; HYDROXYL GROUP; QUINOLIZIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; DRUG STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOSPECIFICITY; SYNTHESIS;

EID: 79951849670     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258415     Document Type: Article

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