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THE REACTION OF CHROMYL CHLORIDE AND O-SILYLATED ENOLATES: A NOVEL REGIOSPECIFIC ROUTE TO α-HYDROXY KETONES.

DOI: 10.1016/S0040-4039(00)88448-8

Source and publish data:

Tetrahedron Letters p. 2917 - 2920 (1982)

Update date:2022-08-17

Topics:

Authors:

Lee, Thomas V.Lee, Thomas V.

Toczek, JudyToczek, Judy

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Article abstract of DOI:10.1016/S0040-4039(00)88448-8

Chromyl chloride reacts regiospecifically with O-silylated enolates to form α-hydroxy ketones.

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Full text of DOI:10.1016/S0040-4039(00)88448-8

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Product name:1-PHENYL-1-TRIMETHYLSILOXYETHYLENE

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