ChemInform Abstract: Synthesis of 4-Aryl-4,5-dihydro-1H-indeno[1,2-d]pyrimidines by Biginelli...

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ChemInform 2011, 42, issue 47 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Fused pyrimidine derivatives R 0515 DOI: 10.1002/chin.201147157 Synthesis of 4-Aryl-4,5-dihydro-1H-indeno[1,2-d]pyrimidines by Biginelli Con- densation and Their Antibacterial Activities. — A variety of new indenopyrimi- dinethiones (V) is synthesized via a multi-component condensation reaction under mi- crowave irradiation conditions. Thiones (IV) and corresponding S-alkylated/S-benzy- lated products are evaluated for their antibacterial activities. S-alkylated indenopy- rimidine derivatives (Va) and (Vb) appear to be the most potent samples. — (KAUR, R.; BANSAL, M.; KAUR*, B.; MISHRA, T.; BHATIA, A.; J. Chem. Sci. (Bangalore, India) 123 (2011) 4, 443-451 ; Dep. Chem., Punjabi Univ., Patiala 147 002, India; Eng.) — C. Cyrus 47- 157

Transcript of ChemInform Abstract: Synthesis of 4-Aryl-4,5-dihydro-1H-indeno[1,2-d]pyrimidines by Biginelli...

Fused pyrimidine derivativesR 0515 DOI: 10.1002/chin.201147157

Synthesis of 4-Aryl-4,5-dihydro-1H-indeno[1,2-d]pyrimidines by Biginelli Con-densation and Their Antibacterial Activities. — A variety of new indenopyrimi-dinethiones (V) is synthesized via a multi-component condensation reaction under mi-crowave irradiation conditions. Thiones (IV) and corresponding S-alkylated/S-benzy-lated products are evaluated for their antibacterial activities. S-alkylated indenopy-rimidine derivatives (Va) and (Vb) appear to be the most potent samples. — (KAUR, R.; BANSAL, M.; KAUR*, B.; MISHRA, T.; BHATIA, A.; J. Chem. Sci. (Bangalore, India) 123 (2011) 4, 443-451 ; Dep. Chem., Punjabi Univ., Patiala 147 002, India; Eng.) — C. Cyrus

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ChemInform 2011, 42, issue 47 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim