File:Acyl Transfer Strategies as Transient Activations for Enantioselective Synthesis (MédiHAL 2279710).jpg
Acyl_Transfer_Strategies_as_Transient_Activations_for_Enantioselective_Synthesis_(MédiHAL_2279710).jpg (455 × 102 pixels, file size: 10 KB, MIME type: image/jpeg)
Captions
Summary
[edit]DescriptionAcyl Transfer Strategies as Transient Activations for Enantioselective Synthesis (MédiHAL 2279710).jpg |
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
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 |
Licensing
[edit]Public domainPublic domainfalsefalse |
This work is in the public domain in France for one of the following reasons:
Please note that moral rights still apply when the work is in the public domain. They encompass, among others, the right to the respect of the author's name, quality and work (CPI art. L121-1). Attribution therefore remains mandatory.
العربية ∙ English ∙ español ∙ français ∙ 日本語 ∙ 한국어 ∙ македонски ∙ русский ∙ Tiếng Việt ∙ 简体中文 ∙ 繁體中文 ∙ +/− |
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 03:50, 20 December 2024 | 455 × 102 (10 KB) | OptimusPrimeBot (talk | contribs) | #Spacemedia - Upload of https://media.hal.science/medihal-02279710/file/Graph_AQ_9.jpg via Commons:Spacemedia |
You cannot overwrite this file.
File usage on Commons
There are no pages that use this file.
Metadata
This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file. The timestamp is only as accurate as the clock in the camera, and it may be completely wrong.
Short title | Acyl Transfer Strategies as Transient Activations for Enantioselective Synthesis |
---|---|
Headline | Acyl Transfer Strategies as Transient Activations for Enantioselective Synthesis |
Author |
|
Image title | 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.dF |
JPEG file comment | CREATOR: gd-jpeg v1.0 (using IJG JPEG v62), quality = 75 |
Keywords |
|