cis- and trans-(4-alkylcyclohexyl)stannanes. Isomers for stereochemical studies of substitution at saturated carbon-tin bonds

Olszowy H.A. and Kitching W. (1984) cis- and trans-(4-alkylcyclohexyl)stannanes. Isomers for stereochemical studies of substitution at saturated carbon-tin bonds. Organometallics, 3 11: 1670-1675.

Author Olszowy H.A.
Kitching W.
Title cis- and trans-(4-alkylcyclohexyl)stannanes. Isomers for stereochemical studies of substitution at saturated carbon-tin bonds
Journal name Organometallics   Check publisher's open access policy
ISSN 0276-7333
Publication date 1984-01-01
Sub-type Article (original research)
Volume 3
Issue 11
Start page 1670
End page 1675
Total pages 6
Subject 1604 Human Geography
1605 Policy and Administration
Abstract The synthesis and characterization of pure cis- and trans-(4-methylcyclohexyl)- and cis- and trans-(4-tert-butylcyclohexyl)triphenylstannanes are described. Their conversion, by hydrochloric acid induced dephenylation-isopropylation, to the corresponding triisopropylstannanes proceeds smoothly to provide stereoisomers capable of providing significant information with respect to brominolysis and trifluoroacetolysis of the carbon-tin bond.
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: Scopus Import - Archived
 
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Created: Tue, 23 Aug 2016, 15:53:38 EST by System User