Base-promoted cascade β-F-elimination/electrocyclization/Diels–Alder/retro-Diels–Alder reaction: efficient access to δ-carboline derivatives-Reference-Cited by-同舟云学术

Base-promoted cascade β-F-elimination/electrocyclization/Diels–Alder/retro-Diels–Alder reaction: efficient access to δ-carboline derivatives

Published:2022 Issue:35 Volume:13 Page:10448-10454
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Sun Xi-Shang¹,Diao Xin-Yu¹,Dong Xiu-Qin¹^ORCID,Wang Chun-Jiang¹²^ORCID

Affiliation:

1. College of Chemistry and Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials, Wuhan University, Wuhan, Hubei, 430072, P. R. China

2. State Key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin, 300071, P. R. China

Abstract

A serendipitous and efficient approach to access various δ-carbolines was developed through base-promoted cascade β-F-elimination/electrocyclization/Diels–Alder/retro-Diels–Alder reaction in good to high yields with excellent regio/chemoselectivity.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Natural Science Foundation of Jiangsu Province

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/SC/D2SC03166C

Reference53 articles.