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Completely stereospecific 1,2-migration of alkyl groups in Et2AlCl promoted pinacol-type rearrangement

✍ Scribed by Gen-ichi Tsuchihashi; Katsuhiko Tomooka; Keisuke Suzuki


Book ID
104233776
Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
257 KB
Volume
25
Category
Article
ISSN
0040-4039

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✦ Synopsis


swnmary:

Completely stereospecific 1,2-migration of alkyl groups was achieved in Et2AlCL- prowted pinacoZ-type rearrangement of chiral B-mesyZoxy alcohols to give optically pure aalkyl ketones including both enantiomers of 4-methyl-3-hexanone, an alarm pheromone of ant.


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