Ac-<scp>l</scp>-methionine-catalyzed, nitrite-triggered cycloaddition reactions between bromides and alkynes/alkenes: step-economical reactions for modular synthesis-Reference-Cited by-同舟云学术

Ac-l-methionine-catalyzed, nitrite-triggered cycloaddition reactions between bromides and alkynes/alkenes: step-economical reactions for modular synthesis

Published:2023 Issue:13 Volume:10 Page:3269-3274
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Shuangrong¹,Ying Zhimin¹,Zhu Qi¹,Zhong Xiuwen¹,Cen Jie¹,Wu You¹,Yu Yongping¹^ORCID,Shao Jiaan²^ORCID,Chen Wenteng¹^ORCID

Affiliation:

1. College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang, 310058, China

2. Key Laboratory of Novel Targets and Drug Study of Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, 310015, China

Abstract

The development of modular, chemically diverse and regioselective reactions for expanding the cycloaddition reaction toolbox hinges heavily on a strict functional 1,3-dipole and dipolarophile pairing exploration.

Funder

Natural Science Foundation of Zhejiang Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00549F

Reference29 articles.

1. Cycloaddition Reactions in Organic Synthesis , ed. S. Kobayashi and K. A. Jørgensen , Wiley , 2001

2. Kinetics and Mechanism of 1,3-Dipolr Cycloadditions

3. 1,3-Dipolar Cycloadditions. Past and Future

4. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

5. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

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