Facile and diastereoselective synthesis of 3,2′-spiropyrrolidine-oxindoles derivatives, their molecular docking and antiproliferative activities

D. Kathirvelan, J. Haribabu, B. S.R. Reddy, C. Balachandran, V. Duraipandiyan

研究成果: Article査読

82 被引用数 (Scopus)

抄録

In the present study, a series of novel highly functionalized spiropyrrolidine-oxindoles have been synthesized through 1,3-dipolar cycloaddition of an azomethine ylide formed from isatin and various amino acids such as sarcosine, proline and thioproline with the dipolarophile (E)-3-(1,3-diphenyl-1H-pyrazol-4-yl)-2-(1H-indole-3-carbonyl)acrylonitrile under optimized conditions. All the synthesized compounds were evaluated for their antimicrobial activity and shown significant activity.

本文言語English
ページ(範囲)389-399
ページ数11
ジャーナルBioorganic and Medicinal Chemistry Letters
25
2
DOI
出版ステータスPublished - 15 1月 2015

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