Asymmetric [3+2]-cyclization of α-imino amide surrogates to construct 3,4-diaminopyrrolidine-2,5-diones-Reference-Cited by-同舟云学术

Asymmetric [3+2]-cyclization of α-imino amide surrogates to construct 3,4-diaminopyrrolidine-2,5-diones

Published:2023 Issue:53 Volume:59 Page:8250-8253
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Ruan Peiran¹,Zhang Cefei¹,Wu Jin¹,Xiao Fengnan¹,Zhang Yongyan¹,Tan Qingfa¹,Su Zhishan¹^ORCID,Feng Xiaoming¹^ORCID,Liu Xiaohua¹^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China

Abstract

Using novel α-imino amide surrogates and chiral guanidine, diaminopyrrolidines derivatives could be obtained with good results and versatile application value. The role of guanidine was demonstrated by DFT calculations.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC01203D

Reference73 articles.

1. Structure-Guided Design of C2-Symmetric HIV-1 Protease Inhibitors Based on a Pyrrolidine Scaffold

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3. Tandem construction of biological relevant aliphatic 5-membered N-heterocycles

4. Tartaric Acid and itsO-Acyl Derivatives. Part 10. Synthesis and Applications of Tartramides, Tartrimides andO-Acyltartramides and Imides

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