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2,2′-Bipyridinium chlorochromate/m-chloroperbenzoic acid-mediated cleavage of cyclic acetals to hydroxyesters

✍ Scribed by Frederick A. Luzzio; Rhiana A. Bobb


Book ID
104256575
Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
166 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


Benzylidene acetals are cleaved to hydroxyesters by means of a reagent system composed of 2,2'-bipyridinium chlorochromate (BPCC) and m-chloroperbenzoic acid. Oxidative cleavage of a 4,6.O-benzylideae glucose derivative affords a 6-O-beazoyl derivative.


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