DIASTEREOSELECTIVE [3+2] CYCLOADDITION OF METHYL 2-PHENLTHIOCYCLOPROPYL KETONE WITH ENOL SILYL ETHERS - SYNTHESIS OF FUNCTIONALIZED CYCLOPENTANES

被引：34

作者：

HORIGUCHI, Y ^{[1
]}

SUEHIRO, I ^{[1
]}

SASAKI, A ^{[1
]}

KUWAJIMA, I ^{[1
]}

机构：

[1] TOKYO INST TECHNOL, DEPT CHEM, MEGURO KU, TOKYO 152, JAPAN

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 38期

关键词：

D O I：

10.1016/S0040-4039(00)61732-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Dimethylaluminum chloride-mediated [3 + 2] cycloaddition of methyl 2-phenylthiocyclopropyl ketone and enol TBDPS or TIPS ethers proceeds highly diastereoselectively to afford functionalized cyclopentanes in good yields.

引用

页码：6077 / 6080

页数：4

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