Cocatalyst-controlled divergent cascade cycloaddition reaction of arylalkynols and dioxopyrrolidienes: access to spiroketals and oxa-bridged eight-membered cyclic ethers-Reference-Cited by-同舟云学术

Cocatalyst-controlled divergent cascade cycloaddition reaction of arylalkynols and dioxopyrrolidienes: access to spiroketals and oxa-bridged eight-membered cyclic ethers

Published:2020 Issue:14 Volume:7 Page:1809-1816
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Hongkai¹²³⁴⁵,Zeng Tianlong¹²³⁴⁵,Li Xinhong¹²³⁴⁵,Wang Songmeng¹²³⁴⁵,Xiao Weiguo¹²³⁴⁵,Liu Lingyan¹²³⁴⁵^ORCID,Chang Weixing¹²³⁴⁵,Li Jing¹²³⁴⁵

Affiliation:

1. The State Key Laboratory and Institute of Elemento-Organic Chemistry

2. College of Chemistry

3. Nankai University

4. Tianjin 300071

5. P. R. China

Abstract

A cocatalyst-controlled divergent cascade cycloaddition reaction was developed for the synthesis of two different complex oxygen-containing heterocyclic compounds from arylalkynols and dioxopyrrolidienes in the presence of Au(i) catalyst.

Funder

National Natural Science Foundation of China

National Basic Research Program of China

Natural Science Foundation of Tianjin City

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00464B

Reference82 articles.

1. Isolation, biological activity and synthesis of benzannulated spiroketal natural products