Journal
JOURNAL OF COMBINATORIAL CHEMISTRY
Volume 12, Issue 4, Pages 582-586Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cc100062e
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Funding
- Foundation of Key Laboratory of Organic Synthesis of Jiangsu Province
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An efficient, convenient, one-pot synthesis of 2,3,3a,4-tetrahydropyrrolo[1,2-a]quinazolin-5(1H)-one and 2,3,3a,4-tetrahydropyrrolo[1,2-a]quinazoline-1,5-dione was accomplished in good yields via the novel reductive cyclization of 2-nitrobenzamides with haloketones or keto acids mediated by SnCl2 center dot 2H(2)O system. A variety of substrates can participate in the process with good yields, making this methodology suitable for library synthesis in drug discovery efforts.
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