Organocatalytic Enantioselective Amination of Morita-Baylis-Hillman Carbonates with Masked Ammonia: A Facile Method for the Synthesis of Unprotected α-Methylene-β-Amino Esters-Reference-Cited by-同舟云学术

Organocatalytic Enantioselective Amination of Morita-Baylis-Hillman Carbonates with Masked Ammonia: A Facile Method for the Synthesis of Unprotected α-Methylene-β-Amino Esters

Published:2011-11-03 Issue:49 Volume:17 Page:13676-13679
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Lin Aijun,Mao Haibin,Zhu Xi,Ge Huiming,Tan Renxiang,Zhu Chengjian,Cheng Yixiang

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201102522/fullpdf

Reference94 articles.

1. Recent Advances in the Baylis−Hillman Reaction and Applications

2. Stereoselective Iodocyclization of 3-Acylamino-2-methylene Alkanoates: Synthesis of Analogues of N-Benzoyl-syn-phenylisoserine

3. Aza-Morita−Baylis−Hillman Reactions and Cyclizations of Conjugated Dienes Activated by Sulfone, Ester, and Keto Groups

4. Pd-Catalyzed Asymmetric Allylic Amination of Morita−Baylis−Hillman Adduct Derivatives Using Chiral Diaminophosphine Oxides: DIAPHOXs

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