Effect of substituents in the carbocyclohexyloxy group on the rate of its cleavage during hydrobrominolysis | Health & Environmental Research Online (HERO)

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Citation
Tags

HERO ID

8702992

Reference Type

Journal Article

Title

Effect of substituents in the carbocyclohexyloxy group on the rate of its cleavage during hydrobrominolysis

Author(s)

Poroshin, KT; Shibnev, VA; Lisovenko, AV; Grechishko, VC

Year

1966

Is Peer Reviewed?

Journal

Bulletin of the Academy of Sciences of the USSR. Division of Chemical Science
ISSN: 0568-5230

Volume

Issue

Page Numbers

880-882

Language

English

DOI

10.1007/BF00849393

Abstract

1. A number of o-methylcarbocyclohexyloxyamino acids and 3,3,5-trimethylcarbocyclohexyloxyglycine were synthesized. 2. The use of the o-methylcarbocyclohexyloxy group as a mixture of isomers leads to a reduction in the hydrobrominolysis rate when compared with the carbocyclohexyloxy group. 3. The presence of three methyl groups in the 3,3,5 position in the cyclohexane ring of the carbocyclohexyloxy group increases the hydrobrominolysis rate when compared with the carbocyclohexyloxy group. 1967 Consultants Bureau.