Year |
Citation |
Score |
2023 |
Khanal HD, Mahato K, Lee YR. Indium(III)-Catalyzed Benzannulation of 3-Formyl-4-pyrones with Terminal Aryl Alkynes: Regioselective Synthesis of Functionalized Salicylaldehydes with -Terphenyl Frameworks. Organic Letters. PMID 37432101 DOI: 10.1021/acs.orglett.3c01810 |
0.47 |
|
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 |
0.663 |
|
2018 |
Gattu R, Bhattacharjee S, Mahato K, Khan AT. Electronic effect of substituents on anilines favors 1,4-addition to trans-β-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles. Organic & Biomolecular Chemistry. PMID 29722779 DOI: 10.1039/C8Ob00736E |
0.655 |
|
2018 |
Mahato K, Arora N, Ray Bagdi P, Gattu R, Ghosh SS, Khan AT. An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I2 and TBHP: access to lead molecules for biomedical applications. Chemical Communications (Cambridge, England). PMID 29364291 DOI: 10.1039/C7Cc08502H |
0.755 |
|
2017 |
Mahato K, Bagdi PR, Khan AT. K2CO3 catalyzed regioselective synthesis of thieno[2,3-b]thiochromen-4-one oximes: access to the corresponding amine and nitroso derivatives. Organic & Biomolecular Chemistry. PMID 28640318 DOI: 10.1039/C7Ob01033H |
0.749 |
|
2015 |
Mahato K, Bagdi PR, Khan AT. Yb(OTf)3 catalysed regioselective synthesis of unusual di- and tri- substituted 3,4-dihydrothiochromeno[3,2-e][1,3]thiazin-5(2H)-one derivatives through a pseudo four-component hetero-Diels–Alder reaction Rsc Advances. 5: 48104-48111. DOI: 10.1039/C5Ra06905J |
0.752 |
|
2015 |
Mahato K, Bagdi PR, Khan AT. ChemInform Abstract: Yb(OTf)3Catalyzed Regioselective Synthesis of Unusual Di- and Tri- Substituted 3,4-Dihydrothiochromeno[3,2-e][1,3]thiazin-5(2H)-one Derivatives Through a Pseudo Four-Component Hetero-Diels-Alder Reaction. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201542192 |
0.756 |
|
2015 |
Mahato K, Ray Bagdi P, Khan AT. ChemInform Abstract: L-Proline-Catalyzed Unusual Product Formation from the Reaction of 4- Hydroxydithiocoumarin and Aldehydes Through a Pseudo-Three-Component Reaction. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201515195 |
0.574 |
|
2014 |
Khan A, Mahato K, Ray Bagdi P. l-Proline-Catalysed Unusual Product Formation from the Reaction of 4- Hydroxydithiocoumarin and Aldehydes through a Pseudo-Three-Component Reaction Synlett. 25: 2438-2441. DOI: 10.1055/S-0034-1379017 |
0.58 |
|
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