An Fe(<scp>iii</scp>)-catalyzed reduction radical tandem strategy to access poly-substituted β-alkenyl valerolactones-Reference-Cited by-同舟云学术

An Fe(iii)-catalyzed reduction radical tandem strategy to access poly-substituted β-alkenyl valerolactones

Published:2023 Issue:6 Volume:10 Page:1551-1556
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Li Fu-Yu¹²³^ORCID,Wang Bei¹²³,Xu Hong¹²³,Xiao Yao¹,Huang Dong-Wei¹,Wang Ji-Yu¹²³^ORCID

Affiliation:

1. Department of Chemistry, Xihua University, China Asymmetric Synthesis and Chiraltechnology Key Laboratory of Sichuan Province, Chengdu 610039, P. R. China

2. Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, P. R. China

3. University of Chinese Academy of Sciences, Beijing 100049, P. R. China

Abstract

The convenient synthesis of structurally diverse and complex poly-substituted β-alkenyl valerolactones is first reported via the reduction radical tandem strategy of 2,3-dienoates and allyl alcohols by Fe(iii)-catalysis.

Funder

Applied Basic Research Program of Sichuan Province

Chengdu Science and Technology Program

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D2QO02038F

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