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[Untitled]

Authors :
N. M. Khvoinova
D. V. Muslin
S. Ya. Khorshev
Source :
Russian Journal of General Chemistry. 71:1799-1801
Publication Year :
2001
Publisher :
Springer Science and Business Media LLC, 2001.

Abstract

The rate and pathway of reactions of 3,5-di-tert-butylbenzoyl trifluoroacetate with tert-butylphenols depend on the number and position of bulky substituents determining the extent of steric shielding of the phenolic hydroxyl.

Subjects

Subjects :
Steric effects
chemistry.chemical_compound
Chemistry
Trifluoroacetic acid
Organic chemistry
General Chemistry
Medicinal chemistry

Details

ISSN :
10703632
Volume :
71
Database :
OpenAIRE
Journal :
Russian Journal of General Chemistry
Accession number :
edsair.doi...........15e44fb127008467a171f2e3f94e8591
Full Text :
https://doi.org/10.1023/a:1013915129700
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