Journal of the Chemical Society (Resumed)

Trans-esterification as a means of halide esterification under neutral conditions

WM Corbett, J Kenner

Index: Corbett; Kenner Journal of the Chemical Society, 1953 , p. 3572,3574

Full Text: HTML

Citation Number: 1

Abstract

THE problem of esterifying alcoholic groupings in molecular structures, eg., glycosides, of which other portions are sensitive to acidic conditions, may be attacked by the procedure of double decomposition, but with only slight success. Thus the preparation of iodides from

Asymmetric alkylation of. beta.-keto esters with optically active sulfonium salts

[Umemura, Kazuyuki; Matsuyama,Haruo; Watanabe, Nobuko; Kobayashi, Michio; Kamigata, Nobumasa Journal of Organic Chemistry, 1989 , vol. 54, # 10 p. 2374 - 2383]

Stereospecific displacement of sulfur from chiral centers. activation via thiaphosphonium salts.

[Krafft, Grant A.; Siddall, Thomas L. Tetrahedron Letters, 1985 , vol. 26, # 40 p. 4867 - 4870]

New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration

[Sevrin, Mireille; Krief, Alain Journal of the Chemical Society, Chemical Communications, 1980 , # 14 p. 656 - 657]