SYNTHESIS OF THE C1-C7 AND C8-C18 SEGMENTS OF ent-AMPHIDININ A

被引：2

作者：

Ishiyama, Haruaki ^{[1
]}

Hangyou, Masahiro ^{[1
]}

Nakatsu, Ayumi ^{[1
]}

Mori, Yuta ^{[1
]}

Kobayashi, Jun'ichi ^{[1
]}

机构：

[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan

来源：

HETEROCYCLES | 2015年 / 90卷 / 02期

关键词：

Amphidinin A; Ampheiniam sp; Dinoflagellate; CATALYTIC ASYMMETRIC EPOXIDATION; SPIN-COUPLING-CONSTANTS; STEREOSELECTIVE-SYNTHESIS; CONFIGURATION; ALDEHYDES; SULFONES; ALCOHOLS; FRAGMENT;

D O I：

10.3987/COM-14-S(K)107

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A stereoselective synthesis of the C1-C7 and C8-C18 segments of the enantiomer of amphidinin A, a cytotoxic polyketide from the culture cells of a symbiotic marine dinoflagellate Amphidinium sp. (strain Y-5), has been achieved, utilizing sulfone-aldehyde coupling, Sharpless asymmetric dihydroxylation, Katsuki-Sharpless asymmetric epoxidation, and Julia-Kocienski olefination.

引用

页码：1254 / 1273

页数：20

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