Asymmetric synthesis of 2-alkyl-substituted 2,5-dihydropyrroles from optically active aza-baylis-hillman adducts. Formal synthesis of (-)-trachelanthamidine

Journal of Organic Chemistry

Volumn 75, Issue 11, 2010, Pages 3578-3586

  Ishikawa, Shingo ^a   Noguchi, Fumiaki ^a   Kamimura, Akio ^a  

^a YAMAGUCHI UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC SYNTHESIS; BAYLIS-HILLMAN ADDUCTS; CIS/TRANS ISOMERS; DIHYDROPYRROLE; FORMAL SYNTHESIS; GOOD YIELD; GRUBBS CATALYSTS; HETEROCYCLIC SYNTHESIS; HIGH YIELD; METATHESIS REACTIONS; OPTICAL PURITY; OPTICALLY ACTIVE; PROTECTIVE GROUP; PYRROLIDINES; REACTION CATALYZED; RING-CLOSURE; SIDE CHAINS; STARTING MATERIALS; SYNTHETIC APPLICATION;

ALKYLATION; ESTERS; HYDROCARBONS; HYDROGENATION; ISOMERS; ORGANIC POLYMERS;

SYNTHESIS (CHEMICAL);

ALCOHOL DERIVATIVE; GUANIDINE DERIVATIVE; LEVO TRACHELANTHAMIDINE; PYRROLE DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CATALYST; RING CLOSING METATHESIS; STEREOCHEMISTRY;

IMINES; OPTICAL ROTATION; PYRROLES; PYRROLIZIDINE ALKALOIDS; SULFONIUM COMPOUNDS;

EID: 77952959980     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100315j     Document Type: Article

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