N-Iodosuccinimide involved one-pot metal-free synthesis of 2-heteroaromatic benzothiazole compounds.

Research paper by Xianglong X Chu, Tiantian T Duan, Xuan X Liu, Lei L Feng, Jiong J Jia, Chen C Ma

Indexed on: 25 Jan '17Published on: 25 Jan '17Published in: Organic & Biomolecular Chemistry

Abstract

A one-pot protocol for the synthesis of structurally diverse 2-hetarylbenzothiazoles via oxidative condensation of the sp(3) C-H bond with benzothiazoles has been described. This process is metal free and operationally simple. A series of 2-hetarylbenzothiazoles were prepared in moderate to good yield under mild conditions.

N-Iodosuccinimide involved one-pot metal-free synthesis of 2-heteroaromatic benzothiazole compounds.

Abstract

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N-Iodosuccinimide involved one-pot metal-free synthesis of 2-heteroaromatic benzothiazole compounds.

Abstract

More like this:

CASSCF and CASPT2 study on O- and Cl-loss predissociation mechanisms of OClO (A(2)A2).

Blue-, green- and non-luminescent crystals from one reaction. Isolation and structural characterization of a series of gold(I)-silver(I) heterometallic complexes utilizing a gold carbene metalloligand containing free amino groups.

Novel Mo(V)-dithiolene compounds: characterization of nonsymmetric dithiolene complexes by electrospray ionization mass spectrometry.

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