Investigations into the enantioselective C-protonation of prostereogenic enolate(s) derived from N,N′-diisopropyl-2-phenylpropanamide using suicide C-based proton sources-Reference-Cited by-同舟云学术

Investigations into the enantioselective C-protonation of prostereogenic enolate(s) derived from N,N′-diisopropyl-2-phenylpropanamide using suicide C-based proton sources

Published:2004-12 Issue:51 Volume:45 Page:9469-9474
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Coumbarides Gregory S.,Eames Jason,Ghilagaber Stephanos,Suggate Michael J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference64 articles.

1. Catalytic Enantioselective Protonation of Enolates

2. Synthesis of (R)-(+)- and (S)-(-)-.alpha.-damascone by tandem Grignard reaction-enantioselective protonation: evidence for the intermediacy of a chiral complex

3. Asymmetric Protonation of Enolates

4. Hydrochloride of chiral piperazine as a chiral proton source

5. Enantioselective protonation of achiral lithium enolates using a chiral amine in the presence of lithium bromide

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