Formal synthesis of (-)-perhydrohistrionicotoxin via cyclic amino acid ester-enolate claisen rearrangement and ring-closing metathesis

Journal of Organic Chemistry

Volumn 70, Issue 14, 2005, Pages 5756-5759

  Kim, Sanghee ^a   Ko, Hyojin ^a   Lee, Taeho ^a   Kim, Deukjoon ^a  

^a Seoul National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; ESTERS; HYDROXYAPATITE;

CLAISEN REARRANGEMENTS; CYCLIC AMINO ACIDS; RING-CLOSING METATHESIS; STEREOGENIC CENTERS;

SYNTHESIS (CHEMICAL);

AMINO ACID; AMINO ACID ESTER ENOLATE; AZASPIROCYCLIC DERIVATIVE; LACTAM; PERHYDROHISTRIONICOTOXIN; UNCLASSIFIED DRUG;

ARTICLE; CLAISEN REARRANGEMENT; RING CLOSING METATHESIS; STEREOCHEMISTRY; SYNTHESIS;

ALCOHOLS; ALKALOIDS; AMINO ACIDS, CYCLIC; AMPHIBIAN VENOMS; AZA COMPOUNDS; CYCLIZATION; ESTERS; LACTAMS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 22144474430     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050608w     Document Type: Article

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