An expedient route to montanine-type amaryllidaceae alkaloids: Total syntheses of (-)-brunsvigine and (-)-manthine

Journal of Organic Chemistry

Volumn 73, Issue 19, 2008, Pages 7580-7585

  Hong, An Wei ^a   Cheng, Tsung Hui ^a   Raghukumar, Vellingiri ^a   Sha, Chin Kang ^a  

^a NATIONAL TSING HUA UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; AMIDES; AMINATION; AMINES; ARSENIC COMPOUNDS; CHEMICAL REACTIONS; CHLORINE COMPOUNDS; COMPLEXATION; CYCLIZATION; HYDROLYSIS; METHYLATION; ORGANIC COMPOUNDS; SUGAR (SUCROSE);

18-CROWN-6; ALLYLIC ALCOHOLS; AMARYLLIDACEAE; ANIONIC CYCLIZATION; CHEMICAL EQUATIONS; DEBENZYLATION; DETOSYLATION; GRIGNARD ADDITION; PICTET-SPENGLER CYCLIZATION; REGIOSELECTIVE CLEAVAGE; STEREOSELECTIVE REDUCTION; SUBSEQUENT HYDROLYSIS; TOTAL SYNTHESIS; TRIFLATE;

SYNTHESIS (CHEMICAL);

ALKALOID DERIVATIVE; BRUNSVIGINE; COCCININE; MANTHINE; MONTANINE; O ACETYLMONTANINE; PANCRACINE; UNCLASSIFIED DRUG;

ARTICLE; BENZYLATION; CHEMICAL REACTION; CYCLIZATION; DRUG SYNTHESIS; ENANTIOMER; GRIGNARD REACTION; HYDROLYSIS; IODINATION; METHYLATION; PICTET SPENGLER REACTION; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

AMARYLLIDACEAE ALKALOIDS; ISOQUINOLINES; QUINIC ACID; STEREOISOMERISM;

EID: 53049108982     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801089y     Document Type: Article

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