A Metal‐Free and Site‐Selective Isothiocyanation of the Allyl C(sp <sup>3</sup> )‐H Bond

Herein, we reported a site‐selective isothiocyanation of allyl C(sp 3 )‐H bonds. Through the hypervalent iodine reagents promotion strategy, selective isothiocyanation of allyl C(sp 3 )‐H bonds in simple cyclic olefins and natural steroid molecules was realized. This method features high site‐selectivity, good functional group tolerance, metal‐free and mild reaction conditions.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-04-15
DOI
https://doi.org/10.1002/adsc.70419
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

A Metal‐Free and Site‐Selective Isothiocyanation of the Allyl C(sp 3 )‐H Bond

Jingyu Meng, Xiaoqian Shen, Fang Wang, Ruixue Ji et al.
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

A Metal‐Free and Site‐Selective Isothiocyanation of the Allyl C(sp 3 )‐H Bond

Jingyu Meng, Xiaoqian Shen, Fang Wang, Ruixue Ji, S. Qian, Zhong‐Quan Liu
article en

Abstract

Herein, we reported a site‐selective isothiocyanation of allyl C(sp 3 )‐H bonds. Through the hypervalent iodine reagents promotion strategy, selective isothiocyanation of allyl C(sp 3 )‐H bonds in simple cyclic olefins and natural steroid molecules was realized. This method features high site‐selectivity, good functional group tolerance, metal‐free and mild reaction conditions.

Advanced Synthesis & CatalysisVol. 368(8)
Nanjing University of Chinese Medicine (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 17%
Catalytic C–H Functionalization Methods
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