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Application of Thio-Ugi Adducts for the Preparation of Benzo[<i>b</i>]thiophene and S‑Heterocycle Library via Copper Catalyzed Intramolecular C–S Bond Formation
Abstract
Fused heterocycles, such as benzo[<i>b</i>]thiophene, thiochroman, benzo[<i>b</i>][1,4]thiazine, and 1,4-benzothiazepine were generated from thio-Ugi adducts containing a thioamide group through copper-catalyzed intramolecular C–S bond formation under microwave irradiation- Text
- Journal contribution
- Biophysics
- Biochemistry
- Cell Biology
- Pharmacology
- Biotechnology
- Cancer
- Hematology
- Plant Biology
- Environmental Sciences not elsewhere classified
- Chemical Sciences not elsewhere classified
- adduct
- benzo
- intramolecular
- FormationFused
- benzothiazepine
- application
- heterocycle
- thioamide group
- thiochroman
- Preparation
- formation
- Catalyzed
- Bond
- microwave irradiation
- Adduct
- Benzo
- Intramolecular
- bond
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Last time updated on 12/02/2018
This paper was published in The Francis Crick Institute.
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