Enantioselective Organocatalytic 1,6-Addition of Azlactones to para-Quinone Methides: An Access to α,α-Disubstituted and β,β-Diaryl-α-amino acid Esters-Reference-Cited by-同舟云学术

Enantioselective Organocatalytic 1,6-Addition of Azlactones to para-Quinone Methides: An Access to α,α-Disubstituted and β,β-Diaryl-α-amino acid Esters

Published:2018-01-24 Issue:4 Volume:20 Page:1142-1145
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Wenjun¹^ORCID,Xu Xianhong¹,Liu Yang¹,Gao Hua¹,Cheng Yuyu²,Li Pengfei²

Affiliation:

1. Department of Medicinal Chemistry, School of Pharmacy, Qingdao University, Qingdao, 266021, China

2. Department of Chemistry, Southern University of Science and Technology, 1088 Xueyuan Blvd., Nanshan District, Shenzhen, Guangdong 518055, China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Special Funds for the Development of Strategic Emerging Industries in Shenzhen

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b00072

Reference55 articles.

1. Unusual Amino Acids: Synthesis and Introduction into Naturally Occurring Peptides and Biologically Active Analogues

2. Peptidomimetics – A Versatile Route to Biologically Active Compounds

3. Interaction of α-Chymotrypsin with Several α-Methyl-α-Acylamino Acid Methyl Esters*

4. Synthesis of [alpha-methyltyrosine-4]angiotensin II: studies of its conformation, pressor activity, and mode of enzymatic degradation.

5. New aspartame-like sweeteners containing L-(αMe)Phe

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