1,7-Acetal Carbon Rearrangementvia1,5-Hydride Transfer in an Oxocanyl Carbenium Ion. Conversion ofO-(5-Hexenyl)-Se,O-heteroacetals orO,O-Acetals into 7-Oxohexanols or 7-Oxohexyl Chlorides-Reference-Cited by-同舟云学术

1,7-Acetal Carbon Rearrangementvia1,5-Hydride Transfer in an Oxocanyl Carbenium Ion. Conversion ofO-(5-Hexenyl)-Se,O-heteroacetals orO,O-Acetals into 7-Oxohexanols or 7-Oxohexyl Chlorides

Published:1993-09 Issue:9 Volume:22 Page:1491-1494
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Yoshimatsu Mitsuhiro,Hatae Noriyuki,Shimizu Hiroshi,Kataoka Tadashi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/22/9/22_9_1491/_pdf

Reference6 articles.

1. Developments in cyclisation reactions

2. Charge as a key component in reaction design. The invention of cationic cyclization reactions of importance in synthesis

3. Generation and Alkylation of .ALPHA.-Lithio-Se,O-heteroacetals, and Stereoselective Cyclization of Olefinic Se,O-Heteroacetals.

4. Preparation of eight-membered cyclic ethers by Lewis acid promoted acetal-alkene cyclizations

5. A general allylation procedure using trimethylallylsilane and fluoride catalysis

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