Enantioselective Conjugate Addition of a Lithium Ester Enolate Catalyzed by Chiral Lithium Amides: A Possible Intermediate Characterized-Reference-Cited by-同舟云学术

Enantioselective Conjugate Addition of a Lithium Ester Enolate Catalyzed by Chiral Lithium Amides: A Possible Intermediate Characterized

Published:2009-04-09 Issue:9 Volume:11 Page:1907-1910
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Lecachey Baptiste¹,Duguet Nicolas¹,Oulyadi Hassan¹,Fressigné Catherine¹,Harrison-Marchand Anne¹,Yamamoto Yasutomo¹,Tomioka Kiyoshi¹,Maddaluno Jacques¹

Affiliation:

1. IRCOF, CNRS UMR 6014 & FR 3038, Université de Rouen, 76821 Mont St. Aignan Cedex, France, and Graduate School of Pharmaceutical Sciences, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol900275y

Reference20 articles.

1. A NMR and Theoretical Study of the Aggregates between Alkyllithium and Chiral Lithium Amides: Control of the Topology through a Single Asymmetric Center

2. Pulsed Gradient Spin−Echo (PGSE) Diffusion and 1H,19F Heteronuclear Overhauser Spectroscopy (HOESY) NMR Methods in Inorganic and Organometallic Chemistry: Something Old and Something New

3. Lithium Diisopropylamide-Mediated Ortholithiation and Anionic Fries Rearrangement of Aryl Carbamates: Role of Aggregates and Mixed Aggregates

4. Solid-State 63Cu and 65Cu NMR Spectroscopy of Inorganic and Organometallic Copper(I) Complexes

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