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Angewandte Chemie - International Edition

Volumn 53, Issue 1, 2014, Pages 272-276

Asymmetric total synthesis of (+)-bermudenynol, a C15 laurencia metabolite with a vinyl chloride containing oxocene skeleton, through intramolecular amide enolate alkylation

(4) Kim, Gyudong a Sohn, Te Ik a Kim, Deukjoon a Paton, Robert S b

a Seoul National University (South Korea)

b UNIVERSITY OF OXFORD (United Kingdom)

Author keywords

intramolecular amide enolate alkylation; natural products; oxocenes; total synthesis

Indexed keywords

ASYMMETRIC TOTAL SYNTHESIS; ENOLATE ALKYLATION; NATURAL PRODUCTS; OXOCENES; RING CLOSING METATHESIS; STEREO-SELECTIVE; TOTAL SYNTHESIS; VINYL CHLORIDES;

AMIDES; CHLORINE COMPOUNDS; METABOLITES; OLEFINS; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

ALKYLATION;

AMIDE; OXOCIN DERIVATIVE;

ALKYLATION; ARTICLE; CHEMISTRY; INTRAMOLECULAR AMIDE ENOLATE ALKYLATION; NATURAL PRODUCTS; OXOCENES; STEREOISOMERISM; SYNTHESIS; TOTAL SYNTHESIS;

INTRAMOLECULAR AMIDE ENOLATE ALKYLATION; NATURAL PRODUCTS; OXOCENES; TOTAL SYNTHESIS;

ALKYLATION; AMIDES; OXOCINS; STEREOISOMERISM;

EID: 84890929596 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201308077 Document Type: Article

Times cited : (35)

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