1997 cleavage reactions, decomposition reactions, pyrolysis cleavage reactions, decomposition reactions, pyrolysis O 0100 26 -050 2,2'-Bipyridinium Chlorochromate/m-Chloroperbenzoic Acid-Mediated Cleavage of Cyclic Acetals to Hydroxyesters. -A reagent system composed of MCPBA and 2,2'-bipyridinium
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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## Abstract Spirocyclic 1,3‐dipolar cycloadducts **1** and **4** of azides to heterocyclic ketene N,N‐acetals open their dihydro‐1,2,3‐triazole ring in the presence of weak Brønsted acids to afford novel 1,3‐substituted triazenes **2**X and **5**X, respectively, which form colorless, crystallized t