Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tushar K Chakraborty"'
Autor:
Parijat Sarkar, Kaleeckal G. Harikumar, Satinder S. Rawat, Sanjib Das, Tushar K. Chakraborty, Amitabha Chattopadhyay
Publikováno v:
Molecules, Vol 26, Iss 13, p 3848 (2021)
Serotonin is a neurotransmitter that plays a crucial role in the regulation of several behavioral and cognitive functions by binding to a number of different serotonin receptors present on the cell surface. We report here the synthesis and characteri
Externí odkaz:
https://doaj.org/article/4a835f0a39fa4633b16bed90baa89ac2
Publikováno v:
ARKIVOC, Vol 2005, Iss 3, Pp 170-178 (2005)
Externí odkaz:
https://doaj.org/article/12fe191397a14b2d871104128b2c3d43
Autor:
Tushar K Chakraborty, Pasunoori Laxman
Publikováno v:
Tetrahedron Letters. 43:2645-2648
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5f1a27548ae0b31dde8c2af1828c6e0
https://doi.org/10.1016/s0040-4039(02)00289-7
https://doi.org/10.1016/s0040-4039(02)00289-7
Publikováno v:
Tetrahedron. 57:9461-9467
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f85ca720a65218e2fa0d73ad546b6221
https://doi.org/10.1016/s0040-4020(01)00940-1
https://doi.org/10.1016/s0040-4020(01)00940-1
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab1fd4a7febd2049b37a0f013caee057
https://doi.org/10.1002/chin.200115233
https://doi.org/10.1002/chin.200115233
Autor:
Tushar K. Chakraborty, Sanjib Das
Indian Institute of Chemical Technology, Hyderabad-500 007, India Manuscript received 6 September 1999 Stereoselective synthesis of the 5,7-acetonide of (2E,5S,6R,7R,8S)-5,7,8-trihydroxy-6-methyl-8-phenyl-2-octenoic acid ethyl ester (3), an isomer of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00b2402d734dff9362980259f7451950
Indian Institute of Chemical Technology, Hyderabad-500 007 Manuscript received 24 August 1998 A simple synthesis of chiral \(\gamma\)-hydroxy-β-methyl methylcarbinols 1 starting from disubstituted olefins 3 is achieved in three steps hydroboration,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c048d4069e1570726be01b53228b0f7f
Indian Institute of Chemical Technology, Hyderabad-500 007 Manuscript received 24 August 1998 A simple synthesis of chiral \(\gamma\)-hydroxy-��-methyl methylcarbinols 1 starting from disubstituted olefins 3 is achieved in three steps hydroborati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efd1d462ec81482950c00cf588eebc1b
Publikováno v:
Chemistry Letters. 26:565-566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fae4bdf96ed54b72c8419cb9f6bf4df1
https://doi.org/10.1246/cl.1997.565
https://doi.org/10.1246/cl.1997.565
Publikováno v:
Chemistry Letters. 26:563-564
Regioselective hydroboration of a 4-methyl-2-alkene, oxidation of the resulting mixture of isomeric alcohols, and finally diastereoselective reduction of the ketone are the key steps in the stereoselective synthesis of C19-C26 fragment of amphidinoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97f967efbbb90a42e9393a4ccc8ade75
https://doi.org/10.1246/cl.1997.563
https://doi.org/10.1246/cl.1997.563