Selective nickel-catalyzed disulfuration of alkyl halides with di/trithiosulfonates-Reference-Cited by-同舟云学术

Selective nickel-catalyzed disulfuration of alkyl halides with di/trithiosulfonates

Published:2024 Issue:11 Volume:11 Page:3196-3203
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Lulu¹,Hou Jiaqi¹,Ma Yingying¹,Wang Hongwei¹,Zhong Yu¹,Liang Fangcan¹,Wang Luyao¹,Wang Qingling²,Liu Ji-Quan¹^ORCID,Xu Wen-Hua¹,Zhu Dianhu¹^ORCID

Affiliation:

1. Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710127, China

2. Shaanxi Natural Carbohydrate Resource Engineering Research Center, College of Food Science and Technology, Northwest University, Xi'an, 710069, China

Abstract

Selective reductive disulfuration of alkyl halides with di/trithiosulfonate reagents was developed through ligand regulation, with key features of broad substrate scope, good tolerance and excellent selectivity to disulfides over trisulfides.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shaanxi Province

Education Department of Shaanxi Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00411F

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