Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes-Reference-Cited by-同舟云学术

Electrocatalytic three-component annulation-halosulfonylation of 1,6-enynes toward 1-indanones using sodium halides as both halogen sources and electrolytes

Published:2020 Issue:13 Volume:22 Page:4259-4269
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhang Tian-Shu¹²³⁴⁵,Hao Wen-Juan¹²³⁴⁵,Wang Rong¹²³⁴⁵,Wang Shi-Chao¹²³⁴⁵,Tu Shu-Jiang¹²³⁴⁵^ORCID,Jiang Bo¹²³⁴⁵^ORCID

Affiliation:

1. School of Chemistry & Materials Science

2. Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials

3. Jiangsu Normal University

4. Xuzhou 221116

5. P. R. China

Abstract

A new electrochemically induced three-component annulation-halosulfonylation of 1,6-enynes has been developed for stereoselective synthesis of 33 examples of 1-indanones with generally good yields under environmentally benign conditions.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/GC/D0GC00771D

Reference75 articles.

1. Visible-light-induced deoxygenative C2-sulfonylation of quinoline N-oxides with sulfinic acids

2. Selectfluor-mediated regioselective nucleophilic functionalization of N-heterocycles under metal- and base-free conditions

3. Metal-free benzannulation of yne-allenone esters for atom economical synthesis of functionalized 1-naphthols