Organocatalytic Enantioselective Conjugate Alkynylation of β-Aminoenones: Access to Chiral β-Alkynyl-β-Amino Carbonyl Derivatives-Reference-Cited by-同舟云学术

Organocatalytic Enantioselective Conjugate Alkynylation of β-Aminoenones: Access to Chiral β-Alkynyl-β-Amino Carbonyl Derivatives

Published:2020-09-23 Issue:19 Volume:22 Page:7427-7432
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Jian-Fei¹,Meng Xin¹,Zhang Chao-Huan²,Yu Chuan-Ming¹^ORCID,Mao Bin²^ORCID

Affiliation:

1. College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, P.R. China

2. Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, P.R. China

Funder

National Natural Science Foundation of China

Zhejiang University of Technology

Natural Science Foundation of Zhejiang Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c02394

Reference64 articles.

1. Synthesis and Reactivity of Propargylamines in Organic Chemistry

2. Potent, Orally Active GPIIb/IIIa Antagonists Containing a Nipecotic Acid Subunit. Structure−Activity Studies Leading to the Discovery of RWJ-53308

3. An efficient synthesis of the orally-active GpIIb/IIIa antagonist FR184764

4. Practical Enantioselective Synthesis of β-Substituted-β-amino Esters

5. Reformatsky Reaction to Alkynyl N-tert-Butanesulfinyl Imines: Lewis Acid Controlled Stereodivergent Synthesis of β-Alkynyl-β-Amino Acids

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