Synthesis of isothiocyanato alkyl sulfides from alkenes using KSCN and DMTSM-Reference-Cited by-同舟云学术

Synthesis of isothiocyanato alkyl sulfides from alkenes using KSCN and DMTSM

Published:2024 Issue:22 Volume:22 Page:4472-4477
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jiang Shixuan¹,Zhuang Daijiao¹,Liu Peihua²,Xu Qiyang¹,Luo Xiaofeng³,Wang Tianqiang³,Zhang Chengcheng¹,Yan Rulong¹^ORCID

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 73000, Gansu, China

2. Research Institute of Oil and Gas Technology of Changqing Oilfield Company, Xian 710018, Shanxi, China

3. Chengdu Guibao Science and Technology Co., Ltd, Chengdu 610041, Sichuan, China

Abstract

A metal-free method to synthesize diversely substituted isothiocyanato alkyl sulfides with KSCN and DMTSM has been developed through the formation of C–NCS and C–S bonds.

Funder

Natural Science Foundation of Gansu Province

Sichuan Province Science and Technology Support Program

Gansu Science and Technology Department

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00487F

Reference66 articles.

1. Insect herbivore counteradaptations to the plant glucosinolate–myrosinase system

2. Zinc-Catalyzed Markovnikov-Type Hydroisothiocyanation of Alkenes with Ammonium Thiocyanate

3. Sulforaphane induces apoptosis in adipocytes via Akt/p70s6k1/Bad inhibition and ERK activation

4. Stable, water extractable isothiocyanates from Moringa oleifera leaves attenuate inflammation in vitro

5. A selective synthesis of β-isothiocyanato ketones through a Staudinger/aza-Wittig reaction of β-azido ketones