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Title: | Indian Journal of Chemistry Sect. B |
Other Titles: | Organic Chemistry including Medicinal Chemistry |
Keywords: | Synthesis and cytotoxic activity of sulfur linked mono / bis heterocycles A variety of sulfur linked mono / bis heterocycles have been prepared and their cytotoxic activity on A549 lung adenocarcinoma cells studied. The imidazolyl and benzimidazolyl thiadiazoles (7c, 8c) display appreciable cytotoxic activity against A549 cells. Metal free synthesis,· docking studies and antimicrobial screening of novel isomeric pyridine substituted thiazole derivatives An approach towards metal free heteroarylation of pyridine, pharmacokinetic properties, in silica studies and in vitro antimicrobial screening results are reported. The practical, efficient, diastereoselective synthesis of (3R,I'S)-3-[(I'-N-methylamino)ethyl]pyrrolidine: from acetylpyrrolidone by asymmetric hydrogenation in 5 steps. A chiral side cbain unit for quinolone type antifungal agents /pe ann-nrngus agents Structure-activity relationship in phenothiazine antipsychotic drugs: Molecular orbital calculation, in silica molecular docking and physico-chemical parameters - A convenient synthesis of enantiomerically pure aisocyano esters and P-Fmoc-amino alkyl isonitriles derived from a-amino acids employing PPh31I2 under mild conditions Synthesis of 4-(2-(substituted phenyl)diazenyl)-Iphenylpyrazolidine- 3,5-dione catalyzed by L-proline and their biological activity 1o In vitro anti-diabetic activity and GC-MS analysis of bioactive compounds present in the methanol extract of Kalanchoe pinnata Synthesis and anti-microbial screening of N-(3- cyano-4,S,6, 7-tetrahydro-l-benzothiop hen-2-y 1)- 2-(arylphenyl)acetamide |
Issue Date: | Sep-2018 |
Publisher: | CSIR-National Institute of Science Communication And Information Resources |
URI: | http://172.16.0.4:8085/heritage/handle/123456789/2513 |
Appears in Collections: | Alerting of New Journals (CHE) |
Files in This Item:
File | Description | Size | Format | |
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Indian Journal of Chemistry Section B.pdf | 2.14 MB | Adobe PDF | View/Open |
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