Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Manas Jana"'
Autor:
Manas Jana, Anup Kumar Misra
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1757-1762 (2013)
A straightforward synthesis of the tetrasaccharide repeating unit of the O-antigen of Escherichia coli O16 has been achieved following a sequential glycosylation strategy. A minimum number of steps was used for the synthesis of the target compound in
Externí odkaz:
https://doaj.org/article/f3e3f2af1af04770a3318a1358a8ec51
Publikováno v:
Journal of Colloid and Interface Science. 498:395-404
Hypothesis The interaction of lysozyme with the N-acetylmuramic acid (NAM) and N-acetylglucosamine (NAG) unit of peptidoglycan (PGN) polymer of the bacterial cell wall is of immense importance to understand the mechanism of lysozyme on PGN. Experimen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::494fe9e03a0016d7f49a9937de8bc0c8
https://doi.org/10.1016/j.jcis.2017.03.060
https://doi.org/10.1016/j.jcis.2017.03.060
Autor:
Vinod K. Nelson, Asif Ali, Naibedya Dutta, Suvranil Ghosh, Subhash C. Mandal, Manas Jana, Subhrangsu Chatterjee, Vibha Dwivedi, Subhash C. Lakhotia, Nihar Ranjan Jana, Anup Kumar Misra, Soumyadip Paul, Gopal Chakrabarti, Andrei P. Komarov, Mahadeb Pal, Arnab Ganguli
Publikováno v:
Oncotarget
// Vinod K. Nelson 1,7,* , Asif Ali 1,* , Naibedya Dutta 1 , Suvranil Ghosh 1 , Manas Jana 1 , Arnab Ganguli 2 , Andrei Komarov 3 , Soumyadip Paul 1 , Vibha Dwivedi 4 , Subhrangsu Chatterjee 5 , Nihar R. Jana 6 , Subhash C. Lakhotia 4 , Gopal Chakrab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932e39c2bd793e08d7bd5cd4e7a070aa
https://doi.org/10.18632/oncotarget.12930
https://doi.org/10.18632/oncotarget.12930
Autor:
Manas Jana, Clay S. Bennett
A synthesis of the nonreducing end hexasaccharide of saccharomicin B, α-(L)-Eva-(1→4)-α-(L)-Eva-(1→4)-α-(L)-Dig- (1→4)-α-(L)-Eva-(1→4)-α-(L)-Dig-(1→4)-β-(D)-Fuc, has been developed. Selective glycosylations of (L)-digitoxose ((L)-Dig)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff81d0e545258ef2284304811b02a404
https://europepmc.org/articles/PMC6465119/
https://europepmc.org/articles/PMC6465119/
Autor:
Manas Jana, Anup Kumar Misra
Publikováno v:
Tetrahedron. 71:3960-3965
A trisaccharide and a tetrasaccharide repeating unit corresponding to the cell wall O-antigen of verotoxin producing Escherichia coli O177 strain have been synthesized in excellent yield using sequential stereoselective glycosylation strategy. A comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5489312b418bb2a745567382410dd05c
https://doi.org/10.1016/j.tet.2015.04.042
https://doi.org/10.1016/j.tet.2015.04.042
Publikováno v:
Tetrahedron: Asymmetry. 25:632-636
A straightforward linear synthetic strategy has been developed for the synthesis of the pentasaccharide repeating unit of the cell wall O-antigenic polysaccharide of enteroadherent Escherichia coli O154 strain. Newly developed glycosylation condition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45fccd7b446156c5652f0673a759c2da
https://doi.org/10.1016/j.tetasy.2014.03.007
https://doi.org/10.1016/j.tetasy.2014.03.007
Publikováno v:
RSC Adv.. 4:37079-37084
A straightforward synthesis of the tetrasaccharide repeating unit of the O-antigen of the Escherichia coli O69 strain as its 2-aminoethyl glycoside has been accomplished by carrying out two iterative glycosylations in one pot. The stereochemical outc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::016ea12146dd1e3e82db2a7d503c6aa1
https://doi.org/10.1039/c4ra06989g
https://doi.org/10.1039/c4ra06989g
Autor:
Susanta Kumar Manna, Shubhankar Samanta, Avijit Jana, Akash Jana, Saikat Kumar Manna, Manas Jana, Bidyut Kumar Senapati, Arabinda Mandal, Suresh Kumar Mondal
Publikováno v:
ChemInform. 47
An efficient synthetic protocol of pyrroles and isoquinolines through NaN3/NH4Cl promoted intramolecular aza-annulation of formyl group with suitable alkenes or alkynes is described in high yield and regioselectivities. The metal free exo-trig and en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97ce656237db44780662e8a78be4b24f
https://doi.org/10.1002/chin.201649129
https://doi.org/10.1002/chin.201649129
Publikováno v:
Carbohydrate research. 434
Novel one-pot reaction conditions have been developed for the preparation of glycosyl thiourea derivatives directly from glycosyl azides mediated by a combination of sulfamic acid and sodium iodide. The reaction conditions were clean, non-toxic and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e92613870dd66a46732246a98750b9
https://pubmed.ncbi.nlm.nih.gov/27639336
https://pubmed.ncbi.nlm.nih.gov/27639336
Autor:
Anup Kumar Misra, Manas Jana
Publikováno v:
Synlett. 23:2789-2794
A series of S -glycosyl N-substituted dithiocarbamate and S -glycosyl S′-substituted trithiocarbonate derivatives have been synthesized under solvent-free conditions. Three-component reaction of glycosyl bromides with carbon disulfide and thiols or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eed1c50aabb165a5c13517c1a82a1901
https://doi.org/10.1055/s-0032-1317521
https://doi.org/10.1055/s-0032-1317521