Saghir Ali - Publications
Affiliations: | IIT Guwahati |
Year | Citation | Score | |||
---|---|---|---|---|---|
2021 | Ali S, Khan AT. An environmentally benign regioselective synthesis of 2-benzyl-4-arylquinoline derivatives using aryl amines, styrene oxides and aryl acetylenes. Organic & Biomolecular Chemistry. 19: 8772-8782. PMID 34591056 DOI: 10.1039/d1ob01699g | 0.657 | |||
2021 | Ali S, Khan AT. Metal-free synthesis of quinoline-2,4-dicarboxylate derivatives using aryl amines and acetylenedicarboxylates through a pseudo three-component reaction. Organic & Biomolecular Chemistry. PMID 34341812 DOI: 10.1039/d1ob01188j | 0.629 | |||
2021 | Ali S, Khan AT. Copper(ii) triflate catalyzed three-component reaction for the synthesis of 2,3-diarylquinoline derivatives using aryl amines, aryl aldehydes and styrene oxides. Organic & Biomolecular Chemistry. 19: 3255-3262. PMID 33885580 DOI: 10.1039/d1ob00125f | 0.721 | |||
2020 | Mondal S, Mahato K, Arora N, Kankane D, Singh UP, Ali S, Khan AH, Ghosh SS, Khan AT. Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity. Organic & Biomolecular Chemistry. PMID 32432294 DOI: 10.1039/D0Ob00054J | 0.631 | |||
2020 | Ali S, Gattu R, Singh V, Mondal S, Khan AT, Dubey G, Bharatam PV. Reaction behaviour of arylamines with nitroalkenes in the presence of bismuth(iii) triflate: an easy access to 2,3-dialkylquinolines. Organic & Biomolecular Chemistry. PMID 32073090 DOI: 10.1039/C9Ob02214G | 0.616 | |||
2018 | Gattu R, Mondal S, Ali S, Khan AT. Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenes. Organic & Biomolecular Chemistry. PMID 30548050 DOI: 10.1039/C8Ob02333F | 0.601 | |||
2016 | Dethe DH, Dherange BD, Ali S, Parsutkar MM. Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D. Organic & Biomolecular Chemistry. PMID 27853800 DOI: 10.1039/C6Ob02322C | 0.367 | |||
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