File:Acyl Transfer Strategies as Transient Activations for Enantioselective Synthesis (MédiHAL 2279710).jpg

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In order to circumvent reactivity or selectivity issues associated with the addition of enolates to electrophiles, chemists have devised innovative methods involving transient activating groups.

Summary

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Description
English: In order to circumvent reactivity or selectivity issues associated with the addition of enolates to electrophiles, chemists have devised innovative methods involving transient activating groups. One of these powerful methods consists of the use of activated ketones, such as -nitroketones, -dicarbonyl compounds or -ketosulfones, with electrophiles possessing a latent hydroxy or amine function. In the presence of a suitable catalyst, an enantioselective addition to the electrophile is facilitated triggering a subsequent Claisen-type fragmentation resulting in an acyl transfer. This subsequent step unveils the desired mono-activated function while directly transferring the ketone, forming in situ on the other side an ester or an amide.
Date Taken on 15 April 2019
Source Acyl Transfer Strategies as Transient Activations for Enantioselective Synthesis
Author

Jean Rodriguez, Adrien Quintard

Adrien Quintard   wikidata:Q81717626
 
Description researcher
Authority file
creator QS:P170,Q81717626
institution QS:P195,Q30295259
institution QS:P195,Q2302586
institution QS:P195,Q3152386
institution QS:P195,Q280413
Keywords
InfoField
Enantioselective synthesis; Organocatalysis; Fragmentation

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Public domain
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