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J Org Chem ; 87(14): 9408-9413, 2022 07 15.
Article in English | MEDLINE | ID: mdl-35758296

ABSTRACT

An approach to diverse cross-benzoin and α-siloxy ketone products which leverages a simple yet underutilized C-C bond disconnection strategy is reported. Acyl substitution of readily accessible α-siloxy Weinreb amides with organolithium compounds enables access to a broad scope of aryl, heteroaryl, alkyl, alkenyl, and alkynyl derivatives. Enantiopure benzoins can be accessed via a chiral pool approach, and the utility of accessible cross-benzoins and α-siloxy ketones is highlighted in a suite of downstream synthetic applications.


Subject(s)
Benzoin , Ketones , Amides/chemistry , Benzoin/chemistry , Ketones/chemistry
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