Intramolecular rearrangements of silenes II . Synthesis of 1-methyl-1-hydro-1-silaacenaphthene from 1-methyl-1-naphthyl-1-silacyclobutane via [4 → 2 + 2]thermocyclodecomposition — transient silene rearrangement sequence. Novel 1,4-hydrogen shift from aryl carbon to sp2 silicon of the silicon-carbon double bond-Reference-Cited by-同舟云学术

Intramolecular rearrangements of silenes II . Synthesis of 1-methyl-1-hydro-1-silaacenaphthene from 1-methyl-1-naphthyl-1-silacyclobutane via [4 → 2 + 2]thermocyclodecomposition — transient silene rearrangement sequence. Novel 1,4-hydrogen shift from aryl carbon to sp2 silicon of the silicon-carbon double bond

Published:1995-04 Issue:1 Volume:492 Page:C4-C7
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Gusel'nikov Leonid E,Volkova Vera V,Lavrukhin Boris D

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference15 articles.

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5. The Chemistry of Organic Silicon Compounds;Raabe,1989

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2. Four-membered Rings with One Silicon, Germanium, Tin, or Lead Atom;Comprehensive Heterocyclic Chemistry III;2008

3. Hetero-π-systems from 2+2 cycloreversions. Part 1. Gusel'nikov–Flowers route to silenes and origination of the chemistry of doubly bonded silicon;Coordination Chemistry Reviews;2003-09

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5. Electronic structure, geometry, and reactivity of arylsilenes: a quantum-chemical study;Russian Chemical Bulletin;1999-02