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Acetaldehyde Silyl Enol Ethers in Enantioselective Mukaiyama Aldol Reactions: Enzyme-Like Organocatalysis in Action.
Dell'Amico, Luca; Zanardi, Franca.
Affiliation
  • Dell'Amico L; Department of Chemical Sciences, Università di Padova, Via Marzolo 1, 35131, Padova, Italy.
  • Zanardi F; Food and Drug Department, Università di Parma, Parco Area delle Scienze 27/A, 43124, Parma, Italy.
Angew Chem Int Ed Engl ; 58(11): 3264-3266, 2019 03 11.
Article in En | MEDLINE | ID: mdl-30730598
ABSTRACT
Touched for the very first time! It is herein highlighted how acetaldehyde silyl enol ethers undergo enantioselective Mukaiyama aldol reaction with aliphatic and aromatic aldehydes. The chemistry relies on the use of the highly efficient and substrate-selective imidodiphosphorimidate catalyst, which displays some of the features of enzymatic catalysis.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2019 Document type: Article Affiliation country:
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