Synthesis of 3-Mono- and 3,5-Difunctionalized Noriceanes (Tetracyclo[5.3.1.02,6.04,9]undecanes)viaOxymetallation of 3,5-Dehydronoriceane (Pentacyclot[5.3.1.02,6.03,5.04,9]undecane). Oxidation of Bicyclo[2.1.0]pentane System by Mercury(II), Thallium(III), and Lead(IV) Acetates.-Reference-Cited by-同舟云学术

Synthesis of 3-Mono- and 3,5-Difunctionalized Noriceanes (Tetracyclo[5.3.1.02,6.04,9]undecanes)viaOxymetallation of 3,5-Dehydronoriceane (Pentacyclot[5.3.1.02,6.03,5.04,9]undecane). Oxidation of Bicyclo[2.1.0]pentane System by Mercury(II), Thallium(III), and Lead(IV) Acetates.

Published:1980-11 Issue:11 Volume:53 Page:3318-3323
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Katsushima Takeo,Yamaguchi Ryohei,Iemura Satoshi,Kawanisi Mituyosi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/53/11/53_11_3318/_pdf

Reference11 articles.

1. The Reaction of 2,4-Dehydrohomoadamantane: The Synthesis of Several 2-Mono- and 2,4-Di-substituted Homoadamantanes

2. Difunctionalized brendanes via thallium triacetate cleavage of the cyclopropyl ring of triaxane

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1. Organic Reactivity Control by Means of Neighboring Groups and Organometallics. A Personal Account;Collection of Czechoslovak Chemical Communications;1994

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4. 3,12-Cycloiceane (pentacyclo[6.3.1.02,4.05,10.07,8]dodecane);Journal of the Chemical Society, Chemical Communications;1987

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