Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bibekananda Jana"'
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
First catalytic and enantioselective conjugate addition of nitromethane to benzylidene-2-benzoyl acetate has been developed using dihydroquinine derived squaramide catalyst with moderate to high selectivities. Asymmetric total synthesis of ABT-627, a
Externí odkaz:
https://doaj.org/article/e4d35fd9ef5040c2868635b9c3bdf3f8
Autor:
Bibekananda Jana, Ajmal Khan, Zia Hashim, Vikas Agarwal, Mansi Gupta, Alok Nath, Mohit Kumar Rai
Publikováno v:
Indian Journal of Tuberculosis. 67:172-176
Objective P-glycoprotein (PGP) overexpression may be one of the operating mechanisms of suboptimal responses to antitubercular treatment (ATT) in patients with lymph node tuberculosis. This might become responsible for the development of drug resista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3473672d81d0077ddbb3c5684b1d9377
https://doi.org/10.1016/j.ijtb.2019.11.015
https://doi.org/10.1016/j.ijtb.2019.11.015
Publikováno v:
Chemistry – A European Journal. 25:14688-14693
Mukaiyama-Mannich reactions of ester enolate equivalents with aldimines have been elegantly used for the asymmetric synthesis of β-amino acids; nevertheless, the corresponding asymmetric reaction employing ketimines are unexplored. Herein, the first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcbe67c10804d1e1575150b9253c66b9
https://doi.org/10.1002/chem.201903512
https://doi.org/10.1002/chem.201903512
Autor:
Saumen Hajra, Bibekananda Jana
Publikováno v:
Organic Letters. 19:4778-4781
A quinine-derived trifunctional sulphonamide catalyst has been developed for the effective asymmetric organocatalytic tandem aza-Henry reaction-cyclization of isatin-derived ketimines and nitroalkane-mesylates for the synthesis of spiro-pyrrolidine/p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34f7f66037c6aa04031b930d8f6b1631
https://doi.org/10.1021/acs.orglett.7b02150
https://doi.org/10.1021/acs.orglett.7b02150
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(64)
Mukaiyama-Mannich reactions of ester enolate equivalents with aldimines have been elegantly used for the asymmetric synthesis of β-amino acids; nevertheless, the corresponding asymmetric reaction employing ketimines are unexplored. Herein, the first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9eebf61a10bcb4907c6d465b285de1c4
https://pubmed.ncbi.nlm.nih.gov/31479157
https://pubmed.ncbi.nlm.nih.gov/31479157
Publikováno v:
ChemInform. 47
A general and direct strategy for the synthesis of chiral spiro-aziridine oxindoles has been developed via an aza-Corey–Chaykovsky reaction of isatin-derived N-tert-butanesulfinyl ketimines with excellent selectivity (dr = 98:2 to >99:1). The metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54ac0b551860e914d6e4297adbe20938
https://doi.org/10.1002/chin.201626124
https://doi.org/10.1002/chin.201626124