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从6-叔丁基富烯到高度官能化的五元环。

From 6-t-butylfulvene to highly functionalized five-membered rings.

作者信息

Baumgartner J, Weber H

机构信息

Institute for Organic Chemistry, Technical University Graz, Stremayrgasse 16, A-8010 Graz, Austria.

出版信息

Chirality. 2001;13(3):159-63. doi: 10.1002/1520-636X(2001)13:3<159::AID-CHIR1014>3.0.CO;2-O.

Abstract

6-t-Butylfulvene was used as the starting material for asymmetric dihydroxylation. The obtained protected diol (2) was used for several stereoselective functionalizations such as epoxidations, hydroboration, and aminohydroxylation. However, these fulvene derivatives proved to be rather unreactive and gave no conversion under, e.g., palladium (0), catalyses or hydroboration conditions.

摘要

6-叔丁基富烯被用作不对称双羟基化的起始原料。所得到的受保护二醇(2)用于多种立体选择性官能团化反应,如环氧化、硼氢化和氨基羟基化反应。然而,这些富烯衍生物被证明反应活性相当低,在例如钯(0)催化或硼氢化条件下没有发生转化。

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