Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/61779
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dc.contributor.authorRane, R A-
dc.contributor.authorMale, R D-
dc.contributor.authorBabhulkar, G V-
dc.contributor.authorSuryawanshi, M R-
dc.contributor.authorKumar, Dileep-
dc.contributor.authorChindhe, S-
dc.contributor.authorPawar, D-
dc.contributor.authorMoharir, S R-
dc.contributor.authorPatil, R K-
dc.date.accessioned2023-04-17T10:30:34Z-
dc.date.available2023-04-17T10:30:34Z-
dc.date.issued2023-04-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/61779-
dc.description313-317en_US
dc.description.abstractMelphalan dimer is an impurity from the synthesis of Melphalan (M216900) which is an antineoplastic agent. In this article, a new route for the synthesis of Melphalan dimer impurity G has been discussed. The new research provides the first high-yield, high-purity synthesis of this impurity. The impurity has been confirmed for purity using HPLC, and its structure has been identified using MS, ¹H and ¹³C NMR.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(04) [Apr 2023]en_US
dc.subjectMelphalanen_US
dc.subjectImpurityen_US
dc.subjectSynthesisen_US
dc.subjectDimer impurityen_US
dc.subjectAntineoplastic agenten_US
dc.titleNovel high yielding route for the synthesis of Melphalan dimer impurity Gen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i4.416en_US
Appears in Collections:IJC Vol.62(04) [Apr 2023]

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