Journal of the American Chemical Society

Stereochemistry of nucleophilic solvent participation in the decomposition of diacyl peroxides

C Walling, JP Sloan

Index: Journal of the American Chemical Society, , vol. 101, p. 7679 - 7683

Full Text: HTML

Citation Number: 8

Abstract

... It is well established that, in a number of cases, the carboxyl inversion process gives a product, RIOCO-OCOR~ with clean retention of configuration at RI.' It occurred to us that an investigation of the stereochemistry of ... 7680 Journal of the American Chemical Society 1 101:26 ...

Related Articles:

Olefin synthesis by reaction of stabilized carbanions with carbene equivalents. 1. Use of (iodomethyl) tributylstannane for methylenation of sulfones

[Pearlman, Bruce A.; Putt, Sterling R.; Fleming, Jeffrey A. Journal of Organic Chemistry, 1985 , vol. 50, # 19 p. 3622 - 3624]

A Free Radical Method for Reduction of Cyclohexanones—Preferential Formation of Equatorial Alcohols

[Synthetic Communications, , vol. 33, # 11 p. 1951 - 1961]

Stereoselective hydrogenation of tert-butylphenols over charcoal-supported rhodium catalyst in supercritical carbon dioxide solvent

[Journal of Catalysis, , vol. 252, # 1 p. 57 - 68]

Synthetic utility and mechanistic studies of the aliphatic reverse Brook rearrangement

[Journal of the American Chemical Society, , vol. 112, # 6 p. 2392 - 2398]

Mechanism of the liquid-phase catalytic hydrogenolysis on palladium/carbon of cyclohexene epoxides

[Journal of Organic Chemistry, , vol. 45, # 21 p. 4139 - 4143]

More Articles...