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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

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

Book ID
126534890
Publisher
Taylor and Francis Group
Year
2007
Tongue
English
Weight
167 KB
Volume
37
Category
Article
ISSN
0039-7911

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📜 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 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 18 KB 👁 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 cyclopropyl lactam
A novel synthesis of cyclopropyl lactam and amide from cis-2-aryl-3-benzoyl-1,1-dicynocyclopropane with H2O2 in the presence of NaHCO3
✍ Zhongjiao Ren; Jie Chen; Yeying Lu; Danyi Wu; Weiguo Cao 📂 Article 📅 2007 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 289 KB

## 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