about
[1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes.Efficient and stereoselective nitration of mono- and disubstituted olefins with AgNO2 and TEMPO.Oxidative trifluoromethylation of unactivated olefins: an efficient and practical synthesis of α-trifluoromethyl-substituted ketones.A Metal-Free Oxidative Dehydrogenative Diels-Alder Reaction for Selective Functionalization of Alkylbenzenes.Sustainable, Oxidative, and Metal-Free Annulation.Catalytic Transfer Hydrogenation Using Biomass as Hydrogen SourceFrontispiece: Sustainable, Oxidative, and Metal-Free AnnulationRadical trideuteromethylation with deuterated dimethyl sulfoxide in the synthesis of heterocycles and labelled building blocksCopper(I)-Catalyzed Radical Addition of Acetophenones to Alkynes in Furan SynthesisCopper-Catalyzed (2+1) Annulation of Acetophenones with Maleimides: Direct Synthesis of CyclopropanesHypervalent Iodine(III) in Direct Carbon–Hydrogen Bond FunctionalizationHypervalent Iodine(III) in Direct Oxidative Amination of Arenes with Heteroaromatic AminesRegioselective annulation of nitrosopyridine with alkynes: straightforward synthesis of N-oxide-imidazopyridinesMetal-Free Annulation of Arenes with 2-Aminopyridine Derivatives: The Methyl Group as a Traceless Non-Chelating Directing GroupOrganocatalytic Oxidative Annulation of Benzamide Derivatives with AlkynesMetal-mediated deformylation reactions: synthetic and biological avenuesipso-Nitration of arylboronic acids with bismuth nitrate and perdisulfatePalladium-catalyzed synthesis of benzofurans and coumarins from phenols and olefinsSynthesis of (E)-nitroolefins via decarboxylative nitration using t-butylnitrite (t-BuONO) and TEMPOEnantio- and Diastereoselective Synthesis of Homopropargyl Amines by Copper-Catalyzed Coupling of Imines, 1,3-Enynes, and Diborons
P50
Q41512513-98456BC5-27C5-4938-9106-7C20A5667AB3Q44321466-81CFFB4D-7C69-4AFC-8816-614D640906E6Q46578195-4F2850F5-50F1-413C-A550-40D0675C04CCQ48259491-AC8ACD9C-1A52-4B23-BC10-34F82E62B00EQ48349357-557577A9-B051-4DA3-A036-D114651AFCEBQ64027904-6ED56DE1-CD3D-46BC-90CA-289664AD21C2Q64027908-043D3698-8D33-4E43-9989-66619A350016Q64027912-EDA57DCC-E603-4823-A970-3C62B1693E75Q64027914-3C7488AF-96A4-436E-93C6-C6677197B620Q64027915-5B009A4D-1D47-4BEE-AB32-FA82382C4711Q64027916-F2BEC5A3-C33B-4555-BC29-23463A27F7B2Q64027917-CBF46F99-EB1B-4B3C-BC72-8D4EB59E5250Q64027922-19F20906-96D0-43F6-8C49-7DAB6D06E44AQ64027926-0BECE443-FFEB-4BE6-B07C-B6AC2BD13B94Q64027930-578DD769-F60F-4029-9AD6-9F252BEE9AE0Q82185032-3823B318-1BB0-4F1B-9165-4588D05FA0FBQ83626511-BB538FA3-A843-4D50-8DDA-F5295B9D8FEDQ86531959-EFDE6230-E628-4C5A-B68C-3ED849B156ECQ86701108-93FB6C1F-D05A-4378-99C7-250811CAE7CFQ92518611-CB9CF978-015A-46C9-BEDD-C763CE0015A0
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Srimanta Manna
@ast
Srimanta Manna
@en
Srimanta Manna
@es
Srimanta Manna
@nl
Srimanta Manna
@sl
type
label
Srimanta Manna
@ast
Srimanta Manna
@en
Srimanta Manna
@es
Srimanta Manna
@nl
Srimanta Manna
@sl
altLabel
Manna
@en
prefLabel
Srimanta Manna
@ast
Srimanta Manna
@en
Srimanta Manna
@es
Srimanta Manna
@nl
Srimanta Manna
@sl
P1053
N-6719-2015
P106
P1153
54784855800
P31
P3829
P496
0000-0002-3903-1256