Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Anup Bhunia"'
Publikováno v:
ACS Catalysis. 13:6704-6709
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eed6b49abc96f348a01f09dc41423e5e
https://doi.org/10.1021/acscatal.3c00958
https://doi.org/10.1021/acscatal.3c00958
Publikováno v:
Chemical Science. 14:2606-2615
Under the influence of mechanical energy, a reduced organic hydrocarbon can transfer electrons in the solid-state to accomplish strong bond activation. Such activation was integrated into a catalytic cycle to design cross-coupling reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44e6e4530916074e6c7185b48d6db085
https://doi.org/10.1039/d2sc06119h
https://doi.org/10.1039/d2sc06119h
Autor:
Armido Studer, Anup Bhunia
Publikováno v:
Chem. 7:2060-2100
Summary This review illustrates pioneering work and recent advancements on the use of pro-aromatic compounds as carbon- and heteroatom-radical precursors. Pro-aromatic systems such as 1,4-cyclohexadienes, dihydronicotinamides, 1,4-dihydropyridines, 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d47c10b4f79d77e2f6c9182e1d96873c
https://doi.org/10.1016/j.chempr.2021.03.023
https://doi.org/10.1016/j.chempr.2021.03.023
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie International Edition
Hydration of alkenes using first row transition metals (Fe, Co, Mn) under oxygen atmosphere (Mukaiyama‐type hydration) is highly practical for alkene functionalization in complex synthesis. Different hydration protocols have been developed, however
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc156cdb7493daec57d3a66d7296dd54
https://doi.org/10.1002/ange.202015740
https://doi.org/10.1002/ange.202015740
Publikováno v:
Organic Letters. 22:4456-4460
Hydrocyanation in the absence of toxic HCN gas is highly desirable. Addressing that challenge, transition-metal-catalyzed transfer hydrocyanation using safe HCN precursors has been developed, but these reagents generally require a Lewis acid for acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bed30e8d247c95801e45b0b829b47b4
https://doi.org/10.1021/acs.orglett.0c01454
https://doi.org/10.1021/acs.orglett.0c01454
Publikováno v:
Chem. 6:512-522
Summary Radical 1,3-trifluoromethylation/alkynylation of various allylboronic esters with concomitant 1,2-boron shift with alkynyl triflones is reported. These chain reactions proceed via CF3-radical addition to the allylic double bond, and the adduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a9c8ec11d6a93503b4ab17dec008816
https://doi.org/10.1016/j.chempr.2019.12.022
https://doi.org/10.1016/j.chempr.2019.12.022
Autor:
Anup Bhunia
Publikováno v:
Chem. 6:320-321
Download : Download high-res image (124KB) Download : Download full-size image Dr. Anup Bhunia is an Alexander von Humboldt postdoctoral fellow working at the Westfalische Wilhelms-Universitat Munster in the lab of Prof. Armido Studer. He received hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::542ab6d633f93ff60a257b01bb4875db
https://doi.org/10.1016/j.chempr.2020.01.017
https://doi.org/10.1016/j.chempr.2020.01.017
Publikováno v:
Journal of the American Chemical Society. 140:16353-16359
Catalytic transfer hydrocyanation represents a clean and safe alternative to hydrocyanation processes using toxic HCN gas. Such reactions provide access to pharmaceutically important nitrile derivatives starting with alkenes and alkynes. Herein, an e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc77da60aabccecb4c43666ec45a4ef4
https://doi.org/10.1021/jacs.8b10651
https://doi.org/10.1021/jacs.8b10651
Autor:
Armido Studer, Anup Bhunia
Publikováno v:
ACS Catalysis. 8:1213-1217
The development of a cross-coupling method for the regioselective β-alkenylation of 2,5-cyclohexadiene carboxylic acid derivatives to form ortho-alkenylarenes through in situ decarboxylation and aromatization is described. The carboxylic acid functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cfa5b8e7cb4fbadd931b5c58e897b9e
https://doi.org/10.1021/acscatal.8b00083
https://doi.org/10.1021/acscatal.8b00083
Autor:
Anup Bhunia, Sumi Joseph, Akkattu T. Biju, Subrata Mukherjee, Rajesh G. Gonnade, Santhivardhana Reddy Yetra
Publikováno v:
Organic & Biomolecular Chemistry. 15:2013-2019
The N-heterocyclic carbene (NHC)-catalyzed enantioselective formal [3 + 2] annulation of α,β-unsaturated aldehydes with 3-hydroxy oxindoles is presented. Under oxidative conditions using the bisquinone oxidant, the reaction resulted in the synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a4332cf0d94d386f6340ee918bd6f9b
https://doi.org/10.1039/c7ob00148g
https://doi.org/10.1039/c7ob00148g