Isothiourea‐Catalyzed Acylative Kinetic Resolution of Tertiary α‐Hydroxy Esters

A highly enantioselective isothiourea‐catalyzed acylative kinetic resolution (KR) of acyclic tertiary alcohols has been developed. Selectivity factors of up to 200 were achieved for the KR of tertiary alcohols bearing an adjacent ester substituent, with both reaction conversion and enantioselectivit...

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Vydáno v:Angew Chem Int Ed Engl
Hlavní autoři: Qu, Shen, Smith, Samuel M., Laina‐Martín, Víctor, Neyyappadath, Rifahath M., Greenhalgh, Mark D., Smith, Andrew D.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2020
Témata:
Research Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7540711/
https://ncbi.nlm.nih.gov/pubmed/32491267
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.202004354
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