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Chemoselective preparation of ketones by the grignard reaction of N-acylpyrazoles

โœ Scribed by Choji Kashima; Isanobu Kita; Katsumi Takahashi; Akira Hosomi


Book ID
112131115
Publisher
Journal of Heterocyclic Chemistry
Year
1995
Tongue
English
Weight
202 KB
Volume
32
Category
Article
ISSN
0022-152X

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๐Ÿ“œ SIMILAR VOLUMES


Preparation of functionalized ketones vi
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S-Chloroketones and 5-oxo-9-decenoic acid methyl ester were prepared from 5-chlorovaleryl chloride and methyl 4-(chloroformyl)-butyrate via Grignard reaction in tetrahydrofuran at -7OO.

Stereoselective Grignard-type reactions
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N~V-Dibenzylamino ketones of the type Bn2N(RI)CHC(O)R 2, prepared in enantiomerically pure form from aamino acids, undergo non-chelation controlled Grignard-type reactions with RLi, RMgX or RCeCI2 without any undesired racemization.