Regiodivergent Enantioselective γ-Additions of Oxazolones to 2,3-Butadienoates Catalyzed by Phosphines: Synthesis of α,α-Disubstituted α-Amino Acids and N,O-Acetal Derivatives-Reference-Cited by-同舟云学术

Regiodivergent Enantioselective γ-Additions of Oxazolones to 2,3-Butadienoates Catalyzed by Phosphines: Synthesis of α,α-Disubstituted α-Amino Acids and N,O-Acetal Derivatives

Published:2015-12-15 Issue:1 Volume:138 Page:265-271
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wang Tianli¹,Yu Zhaoyuan²,Hoon Ding Long¹,Phee Claire Yan¹,Lan Yu²,Lu Yixin¹³

Affiliation:

1. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore

2. School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400030, P. R. China

3. National University of Singapore (Suzhou) Research Institute, 377 Lin Quan Street, Suzhou Industrial Park, Suzhou, Jiangsu P. R. China, 215123

Funder

Economic Development Board - Singapore

GlaxoSmithKline

National University of Singapore

Science and Engineering Research Council, Agency for Science, Technology and Research

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b10524

Reference91 articles.

1. The diverse chemistry of oxazol-5-(4H)-ones

2. Reactivity of Oxazol-5-(4H)-ones and Their Application toward Natural Product Synthesis

3. Stereoselective syntheses of quaternary substituted α-amino acids using oxazol-5-(4H)-ones

4. Oxazolones in Organocatalysis, New Tricks for an Old Reagent

5. The Efficient Direct Synthesis of N,O-Acetal Compounds as Key Intermediates of Discorhabdin A: Oxidative Fragmentation Reaction of α-Amino Acids or β-Amino Alcohols by Using Hypervalent Iodine(III) Reagents

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