DSpace at KIST: A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT INTRAMOLECULAR ESTER ENOLATE ALKYLATION

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A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT INTRAMOLECULAR ESTER ENOLATE ALKYLATION

Authors: KIM, DJ; SHIN, KJ; KIM, IY; PARK, SW

Issue Date: 1994-10-24

Publisher: PERGAMON-ELSEVIER SCIENCE LTD

Citation: TETRAHEDRON LETTERS, v.35, no.43, pp.7957 - 7960

Abstract: (-)-Reiswigin A (1), a novel anti-viral diterpene, has been synthesized in a highly stereoselective manner utilizing a sequential Claisen rearrangement - intramolecular ester enolate alkylation strategy.

Keywords: RELATIVE CONFIGURATION; WITTIG REACTION; ASSIGNMENT; ABSOLUTE; RELATIVE CONFIGURATION; WITTIG REACTION; ASSIGNMENT; ABSOLUTE

ISSN: 0040-4039

URI: https://pubs.kist.re.kr/handle/201004/145480

DOI: 10.1016/S0040-4039(00)78395-X

Appears in Collections:: KIST Article > Others

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