Diastereoselective synthesis of spiro-cyclopropanyl-cyclohexadienones via direct sulfide-catalyzed [2 + 1] annulation of para-quinone methides with bromides-Reference-Cited by-同舟云学术

Diastereoselective synthesis of spiro-cyclopropanyl-cyclohexadienones via direct sulfide-catalyzed [2 + 1] annulation of para-quinone methides with bromides

Published:2020 Issue:22 Volume:18 Page:4257-4266
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Su Yingpeng¹²³⁴^ORCID,Zhao Yanan¹²³⁴^ORCID,Chang Bingbing¹²³⁴^ORCID,Ling Qinqin¹²³⁴,Feng Yawei¹²³⁴,Zhao Xiaolong¹²³⁴,Huang Danfeng¹²³⁴,Wang Ke-Hu¹²³⁴,Huo Congde¹²³⁴^ORCID,Hu Yulai¹²³⁴^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering

2. Northwest Normal University

3. Lanzhou 730070

4. P. R. China

Abstract

A sulfide-catalyzed [2 + 1] annulation of para-quinone methides with diverse bromides was disclosed to access appealing spiro-cyclopropanyl-cyclohexadienones with high diastereoselectivity.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00778A

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