Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Shital K. Chattopadhyay"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2524-2533 (2019)
An alternate synthetic route to the important anticancer drug suberoylanilide hydroxamic acid (SAHA) from its α,ß-didehydro derivative is described. The didehydro derivative is obtained through a cross metathesis reaction between a suitable termina
Externí odkaz:
https://doaj.org/article/3602f68b87dd494c80b8cc23a7d4f03a
Publikováno v:
ACS Omega, Vol 4, Iss 4, Pp 6106-6113 (2019)
Externí odkaz:
https://doaj.org/article/60e7df3b71b64d2fa5c9bcc70235e6c7
Autor:
Nemai Saha, Shital K. Chattopadhyay
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 3104-3110 (2014)
A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps.
Externí odkaz:
https://doaj.org/article/53272a4a3d06494aaeda3352fcac2f91
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 2910-2915 (2013)
A common approach to the important protein kinase inhibitor (−)-balanol and an azepine-ring-modified balanol derivative has been developed using an efficient fragment coupling protocol which proceeded in good overall yield.
Externí odkaz:
https://doaj.org/article/a9f2c62b1a95498abd817528f3c456e4
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05147108e833a58731a06b7f70073762
https://doi.org/10.1002/ejoc.202200391
https://doi.org/10.1002/ejoc.202200391
Autor:
Amrita Ghosh, Shital K. Chattopadhyay
Publikováno v:
Current Microwave Chemistry. 7:123-144
Many medium ring-sized heterocyclic motifs are found in naturally occurring compounds of significant biological activity which led to the investigation of the biological activity of simpler heterocyclic compounds accommodating these ring systems. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c45a225f0d8196c13b32b8379b6ef09f
https://doi.org/10.2174/2213335607666200226101602
https://doi.org/10.2174/2213335607666200226101602
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2524-2533 (2019)
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2524-2533 (2019)
An alternate synthetic route to the important anticancer drug suberoylanilide hydroxamic acid (SAHA) from its α,ß-didehydro derivative is described. The didehydro derivative is obtained through a cross metathesis reaction between a suitable termina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a2bb4d286784f7d84dd190de41aec13
https://doi.org/10.3762/bjoc.15.245
https://doi.org/10.3762/bjoc.15.245
Publikováno v:
Advanced Synthesis & Catalysis. 361:4727-4738
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6588af3762621a8be25c4bc5ef070a5
https://doi.org/10.1002/adsc.201900530
https://doi.org/10.1002/adsc.201900530
Publikováno v:
Bioorganic Chemistry. 123:105766
Eight indolo[3,2-a]phenanthridine derivatives have been synthesized in a regioselective manner involving intramolecular Heck-type arylation as a key step. The compounds display interesting photophysical proprties and hence evaluated for their ability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58966290dce491883361471400ed411a
https://doi.org/10.1016/j.bioorg.2022.105766
https://doi.org/10.1016/j.bioorg.2022.105766
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 3070-3075 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 3070-3075 (2018)
An alternative synthesis of α,ß-unsaturated hydroxamates via cross metathesis between a class-I olefin and N-benzyloxyacrylamide is reported. The reaction proceeds better in the presence of Grubbs’ second generation catalyst within short time and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::349059e9b8535bdc53f76df1c6088524
https://doi.org/10.3762/bjoc.14.285
https://doi.org/10.3762/bjoc.14.285