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A head-to-head comparison of α- and β-alkoxy effects on stereoselectivity. Nucleophilic additions to a cyclohexanone substituted with five axial CO bonds

✍ Scribed by Leo A. Paquette; Jinsung Tae


Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
234 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis


The stereochemical course of the hydride reduction and of the 1,2-addition of allylmagnesium bromide as well as the Normant reagent to 1 has been determined.