Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Tapasi, Kalita"'
Autor:
Rajat Subhra Giri, Srinivasa Rao Manne, Gobinda Dolai, Ashim Paul, Tapasi Kalita, Bhubaneswar Mandal
Publikováno v:
ACS Omega, Vol 2, Iss 10, Pp 6586-6597 (2017)
Externí odkaz:
https://doaj.org/article/3ecbf2810de445ad9eeac3aa68529823
Autor:
Tapasi Kalita, Bhubaneswar Mandal
Publikováno v:
ChemistrySelect. 6:12281-12287
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02ab10adc77757afb8540099f05dcf12
https://doi.org/10.1002/slct.202103006
https://doi.org/10.1002/slct.202103006
Publikováno v:
Asian Journal of Organic Chemistry. 10:1523-1529
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::857f4efd017e9753b099863dfcb55e84
https://doi.org/10.1002/ajoc.202100198
https://doi.org/10.1002/ajoc.202100198
Publikováno v:
Advanced Synthesis & Catalysis. 363:1427-1435
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7d4bb591a09f810533ab1fa606e8cda
https://doi.org/10.1002/adsc.202001416
https://doi.org/10.1002/adsc.202001416
Publikováno v:
ChemistrySelect. 5:12298-12301
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e3145b64eff9cebc6efef65a322fd57
https://doi.org/10.1002/slct.202003078
https://doi.org/10.1002/slct.202003078
Autor:
Srinivasa Rao Manne, Bhubaneswar Mandal, Ashim Paul, Gobinda Dolai, Rajat Subhra Giri, Tapasi Kalita
Publikováno v:
ACS Omega, Vol 2, Iss 10, Pp 6586-6597 (2017)
An efficient, convenient, and selective Lewis acid-based strategy for on-resin deprotection of the side chain tert-butyl-protected aspartic acid and glutamic acid of a peptide is achieved. The method is mild, cost-effective, and Fmoc chemistry compat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7135d0c4e0c194ce62317ef706f76c18
https://doi.org/10.1021/acsomega.7b01143
https://doi.org/10.1021/acsomega.7b01143
Autor:
Tapasi Kalita, Bhubaneswar Mandal, Kishore Thalluri, Nani Babu Palakurthy, Jyoti Chandra, Dharm Dev
Publikováno v:
Asian Journal of Organic Chemistry. 5:663-675
A metal-free and catalytic method for the synthesis of 2-substituted benzoxazoles and benzothiazoles from N-protected amino acids and carboxylic acids is described. The synthesis of benzoxazole on a solid support is demonstrated by the synthesis of b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::659c7938af4d0e9efdd38e90a4d426d9
https://doi.org/10.1002/ajoc.201500527
https://doi.org/10.1002/ajoc.201500527
Publikováno v:
RSC Advances. 5:39692-39696
An operationally simple and metal-free method for the synthesis of a series of trans-4-arylchroman-3-ols via Bronsted acid (TsOH·H2O) catalysed stereoselective intramolecular Friedel–Crafts alkylation of electron-rich arenes by tethered epoxides i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11b2e398627320eb3ffdbbee7e560fa6
https://doi.org/10.1039/c5ra02193f
https://doi.org/10.1039/c5ra02193f
Autor:
Rajat Subhra, Giri, Srinivasa Rao, Manne, Gobinda, Dolai, Ashim, Paul, Tapasi, Kalita, Bhubaneswar, Mandal
Publikováno v:
ACS Omega
An efficient, convenient, and selective Lewis acid-based strategy for on-resin deprotection of the side chain tert-butyl-protected aspartic acid and glutamic acid of a peptide is achieved. The method is mild, cost-effective, and Fmoc chemistry compat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d89a226151780bbbb24c0e28a0290d7a
https://pubmed.ncbi.nlm.nih.gov/31457256
https://pubmed.ncbi.nlm.nih.gov/31457256
Autor:
Jyoti Chandra, Dharm Dev, Tapasi Kalita, Bhubaneswar Mandal, Nani Babu Palakurthy, Kishore Thalluri
Publikováno v:
ChemInform. 47
A metal-free and catalytic method for the synthesis of 2-substituted benzoxazoles and benzothiazoles from N-protected amino acids and carboxylic acids is described. The synthesis of benzoxazole on a solid support is demonstrated by the synthesis of b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee62be551ce0bc5ff04dc6f789903a29
https://doi.org/10.1002/chin.201639140
https://doi.org/10.1002/chin.201639140