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ChemInform Abstract: Protodeboronation of Tertiary Boronic Esters: Asymmetric Synthesis of Tertiary Alkyl Stereogenic Centers.

✍ Scribed by Stefan Nave; Ravindra P. Sonawane; Tim G. Elford; Varinder K. Aggarwal


Publisher
John Wiley and Sons
Year
2011
Weight
53 KB
Volume
42
Category
Article
ISSN
0931-7597

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✦ Synopsis


Abstract

Tertiary boronic esters smoothly undergo protodeboronation in the presence of CsF or TBAF in aqueous solution.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Enantioselective Co
✍ Ravindra P. Sonawane; Vishal Jheengut; Constantinos Rabalakos; Robin Larouche-Ga πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 41 KB

## Abstract Tertiary boronic esters are successfully converted into the homologated alcohols (III) under standard Matteson conditions with complete retention of configuration.

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## Abstract Vinyl, aryl, and alkynyl organometallics add to ketones containing a stereogenic sulfoxide to give tertiary alcohols in diastereo‐ and enantiomerically pure form such as (III) or (VII).