A photo-reagent system of benzimidazoline and Ru(bpy)3Cl2 to promote hexenyl radical cyclization and Dowd–Beckwith ring-expansion of α-halomethyl-substituted benzocyclic 1-alkanones-Reference-Cited by-同舟云学术

A photo-reagent system of benzimidazoline and Ru(bpy)3Cl2 to promote hexenyl radical cyclization and Dowd–Beckwith ring-expansion of α-halomethyl-substituted benzocyclic 1-alkanones

Published:2014-04 Issue:17 Volume:70 Page:2776-2783
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hasegawa Eietsu,Tateyama Minami,Hoshi Tsuneaki,Ohta Taku,Tayama Eiji,Iwamoto Hajime,Takizawa Shin-ya,Murata Shigeru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference108 articles.

1. AlCl3-Promoted Conjugate Reduction of α,β Unsaturated Carbonyl Compounds with 1,3-Dimethyl-2-phenylbenzimidazoline

2. 1,3-Dimethyl-2-phenylbenzimidazoline as a novel and efficient reagent for mild reductive dehalogenation of .alpha.-halo carbonyl compounds and acid chlorides

3. Lewis acid-promoted conjugate reduction of α,β-unsaturated carbonyl compounds by 2-phenylbenzothiazoline (2-phenyl-2,3-dihydrobenzothiazole)

4. New method for the facile reduction of .alpha.-nitro sulfones to nitroalkanes via an electron-transfer-hydrogen atom abstraction mechanism

5. On the mechanism of the reduction of .alpha.-haloketones by 1,3-dimethyl-2-phenylbenzimidazoline. Reduction by a SET (single electron transfer)-hydrogen atom abstraction chain mechanism

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