Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/61932
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dc.contributor.authorJiang, Yu-Rou-
dc.contributor.authorSu, Dan-
dc.contributor.authorWang, Mu-Zhao-
dc.contributor.authorJia, Ai-Quan-
dc.contributor.authorZhang, Qian-Feng-
dc.date.accessioned2023-05-18T05:40:04Z-
dc.date.available2023-05-18T05:40:04Z-
dc.date.issued2023-05-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/61932-
dc.description425-430en_US
dc.description.abstractCondensation of 2-nitrobenzaldehyde with five amino acid compounds (valine, glycine, leucine, aspartic acid, and glutamic acid) gives the corresponding Schiff bases, which upon treatment with sodium borohydride afford the reductive amination products 1−5. Compounds 1−5 have been well characterized by FT-IR and 1H NMR spectroscopic techniques, in addition to X-ray crystallography, from which the structure of compound 2 has been established. Compound 2 crystallizes in monoclinic space group P21/c, with a = 12.215(8), b = 8.096(5), c = 10.608(7) Å, β = 115.324(7), and Z = 4.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.62(05) [May 2023]en_US
dc.subject2-Nitrobenzaldehydeen_US
dc.subjectAmino aciden_US
dc.subjectSchiff baseen_US
dc.subjectReductive aminationen_US
dc.subjectX-ray structureen_US
dc.titleSyntheses and characterizations of 2-nitrobenzaldehyde amino acid Schiff base reductive amination compoundsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i5.1408en_US
Appears in Collections:IJC Vol.62(05) [May 2023]

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