A strategic approach to the synthesis of functionalized spirooxindole pyrrolidine derivatives: in vitro antibacterial, antifungal, antimalarial and antitubercular studies. (6th November 2014)

• Record Type: Journal Article
• Authors: Haddad, Saoussen; Boudriga, Sarra; Akhaja, Tarunkumar Nanjibhai; Raval, Jignesh Priyakant; Porzio, François; Soldera, Armand; Askri, Moheddine; Knorr, Michael; Rousselin, Yoann; Kubicki, Marek M.; Rajani, Dhanji
• Is Part Of: New journal of chemistry. Volume 39:Number 1(2015:Jan.)
• Page Start: 520
• Page End: 528
• Publication Date: 2014-11-06
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c4nj01008f
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : A series of spirooxindole pyrrolidine derivatives has been synthesized and evaluated for their in vitro biological activities. The observed regio- and stereoselectivity of the cycloaddition reaction has been rationalized using DFT calculations. Abstract : A series of spiro[pyrrolidin-2, 3′-oxindoles] has been synthesized by exo -selective 1, 3-dipolar cycloaddition reaction of a stabilized azomethine ylide, generated in situ by thermal [1, 5]-prototropy, across various ( E )-3-arylidene-1-phenyl-pyrrolidine-2, 5-diones. The stereochemistry of these N-heterocycles has been confirmed using an X-ray diffraction study. To rationalize the observed regio- and stereoselectivity, DFT calculations at the B3LYP/6-31G(d, p) level were employed. It was found that this reaction preferentially affords the kinetic product. The compounds have been screened for their in vitro antibacterial, antifungal, antimalarial and antitubercular activities. Several compounds exhibited good activities comparable to those of established standard drugs.