期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 14, 期 2, 页码 582-589出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ob01790d
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资金
- SERB-DST New Delhi [SB/EMEQ-075/2013]
- UGC, New Delhi
The synthesis of 2-sulfenylimine chromene compounds (8) is accomplished by reacting benzaldehyde (1), malanonitrile (2) and dimedone (3) followed by sequential addition of N-chlorosuccinimide and thiophenols to the in situ formed 2-amino-4(H) chromenes (4) in a one pot, catalyst free, five component reaction in toluene medium. When aniline was employed as the nucleophile in place of thiophenol, the formation of hexahydrobenzofuran-2-N-phenyl carboxamide derivatives (5) was observed. Excellent yields, simple reaction conditions and high compatibility are the advantages of this protocol.
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