Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Rahul D. Kamble"'
Publikováno v:
Current Research in Green and Sustainable Chemistry, Vol 5, Iss , Pp 100268- (2022)
This protocol involves the NH4Cl catalyzed Pictet−Spengler reactions of tryptamine and arylaldehydes in anhydrous MeOH solvent to gives corresponding tetrahydro-β-carbolines (THβC) with 90% yield. This methodology offers mild, efficient and green
Externí odkaz:
https://doaj.org/article/2b540a915a9847a9a30451f11c7cdf34
Autor:
Rahul D. Kamble, Milind V. Gaikwad, Manojkumar R. Tapare, Shrikant V Hese, Shuddhodan N Kadam, Bhaskar S. Dawane, Ajay N Ambhore
An efficient and convenient method has been developed for the synthesis of 2- amino-5-oxo-4-phenyl-4, 5-dihydropyrano[3,2-c]chromene-3-carbonitrile derivatives from a one-pot multi-component reaction between 4-hydroxy-2H- chromen-2-one. Aromatic alde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::161330da9c17ed418c96a6c8f5794e56
https://zenodo.org/record/5920233
https://zenodo.org/record/5920233
Autor:
Rajesh N. Gacche, Sonali S. Kamble, Bhaskar S. Dawane, Rohan J. Meshram, Kapil K. Patil, Shrikant V. Hese, Pratima P. Mogle, Rahul D. Kamble
Publikováno v:
Medicinal Chemistry Research. 26:805-818
Diabetes is embracing the human population in logarithmic fashion both in developed as well as developing countries. Aldose reductase is one of the important enzymes of polyol pathway of sugar metabolism in humans. Aldose reductase inhibition has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::996d7eeb01ff2f802143d7b76febc213
https://doi.org/10.1007/s00044-017-1794-0
https://doi.org/10.1007/s00044-017-1794-0
Autor:
Rahul D. Kamble, Shuddhodan N. Kadam, Ajay N. Ambhore, Shrikant V. Hese, Bhaskar S. Dawane, Madhav J. Hebade, Milind V. Gaikwad
Publikováno v:
European Journal of Chemistry. 7:431-435
The present report describes a microwave assisted convenient and efficient protocol for the synthesis of new 6-(4-substituted-phenyl)-3-methylimidazo[2,1- b ]thiazole-2-carbohydra- zide derivatives. The current method holds a tag of green synthesis b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a8dbd6cc6c0db2dc9f55120b34dc764
https://doi.org/10.5155/eurjchem.7.4.431-435.1485
https://doi.org/10.5155/eurjchem.7.4.431-435.1485
Autor:
Rajesh N. Gacche, Rohan J. Meshram, Shuddhodan N. Kadam, Madhav J. Hebade, Sonali S. Kamble, Ajay N. Ambhore, Rahul D. Kamble, Milind V. Gaikwad, Bhaskar S. Dawane, Shrikant V. Hese
Publikováno v:
Computational biology and chemistry. 80
Development of novel, safe and effective drug candidates combating the emerging drug resistance has remained a major focus in the mainstream of anti-tuberculosis research. Here, we inspired to design and synthesize series of new pyridin-4-yl-1,3,4-ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d873a915938c44bac8ffce0a5eb4f50d
https://pubmed.ncbi.nlm.nih.gov/30901601
https://pubmed.ncbi.nlm.nih.gov/30901601
Autor:
Shrikant V. Hese, Shuddhodan N. Kadam, Madhav J. Hebade, Ajay N. Ambhore, Pratima P. Mogle, Rahul D. Kamble, Bhaskar S. Dawane
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 191:1155-1159
An efficient, green, rapid multitasking protocol for the selective C-5 substitution of 2-aminothiazole using iodic acid and aqueous PEG-400 was developed. The method found suitable for C-5 substitution i.e. iodination and thiocyanation of 2-amino thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee3fdd50e1fc4239a384e28edf5fbcd5
https://doi.org/10.1080/10426507.2016.1149851
https://doi.org/10.1080/10426507.2016.1149851
Autor:
Rahul A. More, Shrikant V. Hese, Rajesh N. Gacche, Bhaskar S. Dawane, Sonali S. Kamble, Rohan J. Meshram, Rahul D. Kamble
Publikováno v:
Computational Biology and Chemistry. 61:86-96
Display Omitted Efficient one-pot synthesis of thiazole bearing pyrazole derivatives.Compound showing selective COX-II inhibition.Molecular docking is in agreement with experimental COX-II assay.Analysis of protein-ligand interaction patterns with CO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8121612289cfbb89499428bbdcddb837
https://doi.org/10.1016/j.compbiolchem.2016.01.007
https://doi.org/10.1016/j.compbiolchem.2016.01.007
Publikováno v:
Research on Chemical Intermediates. 41:7541-7551
A green, efficient, and simple method for synthesis of 5,6,7,8-tetrahydroquinoline-3-carbonitrile derivatives via one-pot three-component condensation of 2,6-bis(substituted benzylidene)cyclohexanone, arylamines/substituted 2-aminothiazoles, and malo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a913da13cfb63b45970315d56591b24
https://doi.org/10.1007/s11164-014-1842-z
https://doi.org/10.1007/s11164-014-1842-z
Autor:
Rajesh N. Gacche, Rahul D. Kamble, Bhaskar S. Dawane, Shrikant V. Hese, Rohan J. Meshram, Jivan R. Kote
Publikováno v:
Medicinal Chemistry Research. 24:1077-1088
In the midst of increasing multidrug resistance and the growing incidence of infections of Mycobacterium tuberculosis, there is compelling evidence for the synthesis of novel and effective anti-tuberculosis agents. In this report, we have synthesized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d978888660c8086ebfad1eb92d9e2506
https://doi.org/10.1007/s00044-014-1165-z
https://doi.org/10.1007/s00044-014-1165-z