Access to azonanes via Pd-catalyzed decarboxylative [5 + 4] cycloaddition with exclusive regioselectivity-Reference-Cited by-同舟云学术

Access to azonanes via Pd-catalyzed decarboxylative [5 + 4] cycloaddition with exclusive regioselectivity

Published:2021 Issue:24 Volume:8 Page:7004-7008
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Yin¹²,He Yicheng²,Liu Yang²,Wei Kun¹,Guo Wusheng²³^ORCID

Affiliation:

1. School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, China

2. Frontier Institute of Science and Technology (FIST), Xi'an Jiaotong University, Xi'an 710045, China

3. School of Chemistry, Xi'an Key Laboratory of Sustainable Energy Materials Chemistry, and MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, Xi'an Jiaotong University, Xi'an 710049, China

Abstract

An efficient approach for the synthesis of azonanes via Pd-catalyzed decarboxylative [5 + 4] cycloaddition has been developed. The reactions feature wide functional group tolerance with exclusive regioselectivity.

Funder

Xi’an Jiaotong University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO01405F

Reference48 articles.

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3. Synthesis and Biological Evaluation of a New Family of Constrained Azabicyclic Homocholine Analogues