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The reaction of chromyl chloride and O-silylated enolates: a novel regiospecific route to α-hydroxy ketones.

✍ Scribed by Thomas V Lee; Judy Toczek

Publisher: Elsevier Science
Year: 1982
Tongue: French
Weight: 166 KB
Volume: 23
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)88448-8

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✦ Synopsis

Swrunary: ChromyZ chloride reacts regiospecifically with 0-silylated enolates to form cc-hydroxy ketones.

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