Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Arup Maiti"'
Autor:
Ashis Roy, Tonmoy Sarkar, Sebak Datta, Arup Maiti, Monali Chakrabarti, Trisha Mondal, Chaitali Mondal, Apurba Banerjee, Subhasis Roy, Soumen Mukherjee, Pragati Muley, Sabyasachi Chakraborty, Manish Banerjee, Mrinalkanti Kundu, Kuldeep K. Roy
Publikováno v:
Chemical Biology & Drug Design. 99:496-503
Inhibition of extracellular secreted enzyme autotaxin (ATX) represents an attractive strategy for the development of new therapeutics to treat various diseases and a few inhibitors entered in clinical trials. We herein describe structure-based design
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::598802decc6082841d6188d0c659f5b8
https://doi.org/10.1111/cbdd.14017
https://doi.org/10.1111/cbdd.14017
Autor:
Rahul Gajbhiye, Kuldeep K. Roy, Jayatri Naskar, Mushtaq Ahmad Wani, Arnish Chakraborty, Pranab Dhar, Arup Maiti, Soumen Mukherjee, Rajib Barik, Ashis Roy, Susanta Kumar Mondal, Chhanda Rarhi, Mrinalkanti Kundu, Susanta Adhikari, Priyadarshi Manna
Publikováno v:
ChemistrySelect. 5:4559-4566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20c1d4863f074cef0f7bc0a058e9ca8d
https://doi.org/10.1002/slct.202000208
https://doi.org/10.1002/slct.202000208
Publikováno v:
Synthesis. 51:3231-3240
A new, convenient synthesis of dibenzo[b,e]azepin-6-ones and seven-membered sultam derivatives have been envisaged via Pd-catalyzed regioselective intramolecular Heck reaction of the corresponding easily accessible precursors. This protocol has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17051d8134dfa3413164dea0330235b8
https://doi.org/10.1055/s-0037-1611548
https://doi.org/10.1055/s-0037-1611548
Autor:
Jhillu S. Yadav, Arup Maiti
Publikováno v:
Tetrahedron. 58:4955-4961
A stereoselective syntheses of panaxytriol 1 and panaxydol 2 from d -arabinose using base induced double elimination of 4,5-O-isopropylidene propargyl chloride as a key step is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d6b0b6c0285b4b3615e0f8009d5a856
https://doi.org/10.1016/s0040-4020(02)00423-4
https://doi.org/10.1016/s0040-4020(02)00423-4
Publikováno v:
The Journal of Organic Chemistry. 66:8370-8378
We describe for the first time the free radical cyclization of enantiomerically pure alkyne-tethered aldehydes obtained from a carbohydrate (6, 7). The synthesis of compounds 6 and 7 obtained from a derivative of D-ribose is reported. These radical p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a6254180270b336713bf1dac2a2953e
https://doi.org/10.1021/jo010455m
https://doi.org/10.1021/jo010455m
Autor:
Jhillu S. Yadav, Arup Maiti
Publikováno v:
Tetrahedron Letters. 42:3909-3912
An efficient protocol for the synthesis of chiral polyhydroxy diacetylenic alcohols from chiral 4,5- O -isopropylidene propargyl chlorides using strong bases is described and is useful for the synthesis of biologically active natural products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e7d9d3fc574ef146cffdeab1a70973b
https://doi.org/10.1016/s0040-4039(01)00580-9
https://doi.org/10.1016/s0040-4039(01)00580-9
Autor:
Jhillu S. Yadav, Arup Maiti
Publikováno v:
Synthetic Communications. 31:1499-1506
Benylic, allylic, and propargylic alcohols, as well as diols, can be oxidized with o-iodoxybenzoic acid (IBX) in the presence of stabilized Wittig ylide[1] to generate α,β-unsaturated ester in one pot. This is useful when the intermediate aldehydes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::196c9de232be4db55b0e1240af6488e5
https://doi.org/10.1081/scc-100104061
https://doi.org/10.1081/scc-100104061
Autor:
Arup Maiti, Jhillu S. Yadav
Publikováno v:
ChemInform. 32
Benylic, allylic, and propargylic alcohols, as well as diols, can be oxidized with o-iodoxybenzoic acid (IBX) in the presence of stabilized Wittig ylide[1] to generate α,β-unsaturated ester in one pot. This is useful when the intermediate aldehydes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90dc78acb69a1edbbf26b877ed5101bd
https://doi.org/10.1002/chin.200144070
https://doi.org/10.1002/chin.200144070
Autor:
Arup Maiti, Jhillu S. Yadav
Publikováno v:
ChemInform. 32
An efficient protocol for the synthesis of chiral polyhydroxy diacetylenic alcohols from chiral 4,5- O -isopropylidene propargyl chlorides using strong bases is described and is useful for the synthesis of biologically active natural products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f1702e1464325258516305375960792
https://doi.org/10.1002/chin.200135067
https://doi.org/10.1002/chin.200135067
Publikováno v:
ChemInform. 33
Trityl ethers are chemoselectively deprotected to the corresponding alcohols in high yields by a catalytic amount of indium tribromide in aqueous acetonitrile. The method is compatible with various functional groups such as acetonides, acetates, benz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5c073a6dd45dbbb567dfa5afc63d63d
https://doi.org/10.1002/chin.200223066
https://doi.org/10.1002/chin.200223066