Transition‐Metal‐Free Cross‐Coupling of Arylsilanes with DAST Reagent: Synthesis of Aromatic Sulfinamides | Zendy

Liu Zhenwei | Zendy; Liu Xinya | Zendy; Luan Nannan | Zendy; Geng Yang | Zendy; Liang Apeng | Zendy; Li Jingya | Zendy; Zou Dapeng | Zendy; Wu Yusheng | Zendy; Wu Yangjie | Zendy

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Transition‐Metal‐Free Cross‐Coupling of Arylsilanes with DAST Reagent: Synthesis of Aromatic Sulfinamides

Author(s) -

Liu Zhenwei,

Liu Xinya,

Luan Nannan,

Geng Yang,

Liang Apeng,

Li Jingya,

Zou Dapeng,

Wu Yusheng,

Wu Yangjie

Publication year - 2020

Publication title -

chemistryselect

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 34

ISSN - 2365-6549

DOI - 10.1002/slct.201904464

Subject(s) - reagent , chemistry , substrate (aquarium) , scope (computer science) , transition metal , combinatorial chemistry , coupling (piping) , organic chemistry , materials science , catalysis , computer science , metallurgy , oceanography , programming language , geology

A transition‐metal‐free cross‐coupling of arylsilanes with DAST (diethylaminosulfur trifluoride) reagent has been developed. A number of aromatic sulfinamides were obtained in reasonable yields (15%‐87%). Notable advantages of this method include easy operation, mild reaction conditions and wide substrate scope.

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