𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A novel synthesis of cyclopropyl lactam and amide from cis-2-aryl-3-benzoyl-1,1-dicynocyclopropane with H2O2 in the presence of NaHCO3

✍ Scribed by Zhongjiao Ren; Jie Chen; Yeying Lu; Danyi Wu; Weiguo Cao

Publisher
Journal of Heterocyclic Chemistry
Year
2007
Tongue
English
Weight
289 KB
Volume
44
Category
Article
ISSN
0022-152X

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

magnified image

The process for preparation of cyclopropyl lactam and amide from cis‐2‐aryl‐3‐benzoyl‐1,1‐dicynocyclopropane with H~2~O~2~ in the Presence of NaHCO~3~ is described. The highly stereoselective conversion of monocyano group to amide has been carried out in the present method.

πŸ“œ SIMILAR VOLUMES

Novel Procedure for Highly Stereoselecti
Novel Procedure for Highly Stereoselective Synthesis of Bicyclic Cyclopropane-lactam with cis-2-Aryl-1-benzoyl-3,3-dicyanocyclopropane and 2-Cyanomethyl-1,3-benzothiazole in Water.
✍ Zhongjiao Ren; Weiguo Cao; Jie Chen; Yeying Lu πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons βš– 18 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

A novel synthesis of 5-aryl-3-phenylpyra
A novel synthesis of 5-aryl-3-phenylpyrazole from 2-aryl-3-benzoyl-1,1-cyclopropanedicarbonitrile and hydrazine
✍ Zhongjiao Ren; Weiguo Cao; Jie Chen; Yu Wang; Weiyu Ding πŸ“‚ Article πŸ“… 2006 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 427 KB πŸ‘ 1 views

A new process for synthesis of 5-aryl-3-phenylpyrazole is achieved. The regioselective ring-opening reaction of 2-aryl-3-benzoyl-1,1-cyclopropanedicarbonitrile with hydrazine plays a crucial role in the described process.