Ring-closing metathesis in the synthesis of fused sultones

被引：23

作者：

Mondal, Shovan ^{[1
]}

Debnath, Sudatshan ^{[1
]}

机构：

[1] Visva Bharati Univ, Dept Chem, Santini Ketan 731235, W Bengal, India

来源：

TETRAHEDRON LETTERS | 2014年 / 55卷 / 09期

关键词：

Ring closing metathesis; Grubbs' II catalyst; Claisen rearrangement; Vinyl sulfonates; Sultones; ENANTIOSELECTIVE TOTAL-SYNTHESIS; IDENTIFICATION;

D O I：

10.1016/j.tetlet.2014.01.074

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Synthesis of seven-membered sultones fused with different carbo- and heterocycles have been developed using ring closing metathesis as the key operation. The required substrates have been easily synthesized from their commercially available corresponding phenols. (c) 2014 Elsevier Ltd. All rights reserved.

引用

页码：1577 / 1580

页数：4

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