about
Nitro-Mannich reaction.Enantiospecific Alkynylation of Alkylboronic Esters.Short Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line Synthesis.Enantiospecific Trifluoromethyl-Radical-Induced Three-Component Coupling of Boronic Esters with Furans.Photoredox α-vinylation of α-amino acids and N-aryl amines.Merging photoredox and nickel catalysis: decarboxylative cross-coupling of carboxylic acids with vinyl halides.Enantiospecific sp2 -sp3 Coupling of ortho- and para-Phenols with Secondary and Tertiary Boronic Esters.Visible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ-Amino Boronic Esters.Enantiospecific Three-Component Alkylation of Furan and Indole.NMR chemical shifts of molecules encapsulated in single walled carbon nanotubes.Stereo- and Regiocontrolled Methylboration of Terminal Alkynes.Enantiodivergent Synthesis of Allenes by Point-to-Axial Chirality Transfer.Chiral Aniline Synthesis via Stereospecific C(sp)-C(sp) Coupling of Boronic Esters with Aryl HydrazinesSynthesis of Functionalized Cyclopropanes from Carboxylic Acids by a Radical Addition-Polar Cyclization CascadeSynthesis of Functionalized Cyclopropanes from Carboxylic Acids by a Radical Addition-Polar Cyclization CascadePhotoinduced Deaminative Borylation of AlkylaminesEnantiodivergent Synthesis of Allenes by Point-to-Axial Chirality TransferVisible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ-Amino Boronic EstersEnantiospecific sp2 -sp3 Coupling of ortho - and para -Phenols with Secondary and Tertiary Boronic EstersEnantiospecific Trifluoromethyl-Radical-Induced Three-Component Coupling of Boronic Esters with FuransShort Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line SynthesisEnantiospecific Alkynylation of Alkylboronic EstersEnantiospecific Synthesis of ortho -Substituted 1,1-Diarylalkanes by a 1,2-Metalate Rearrangement/anti -S N 2′ Elimination/Rearomatizing Allylic Suzuki-Miyaura Reaction SequenceEnantiospecific Synthesis of ortho -Substituted 1,1-Diarylalkanes by a 1,2-Metalate Rearrangement/anti -S N 2′ Elimination/Rearomatizing Allylic Suzuki-Miyaura Reaction SequenceComplex Boron-Containing Molecules through a 1,2-Metalate Rearrangement/anti-S N 2′ Elimination/Cycloaddition Reaction SequenceCatalyst-Free Deaminative Functionalizations of Primary Amines by Photoinduced Single-Electron TransferPhotoredox-Catalyzed Cyclobutane Synthesis by a Deboronative Radical Addition-Polar Cyclization CascadeReductive nitro-Mannich route for the synthesis of 1,2-diamine containing indolines and tetrahydroquinolinesDivergent, Stereospecific Mono- and Difluoromethylation of Boronic EstersRing-Opening Lithiation-Borylation of 2-Trifluoromethyl Oxirane: A Route to Versatile Tertiary Trifluoromethyl Boronic EstersMethylenespiro[2.3]hexanes via Nickel-Catalyzed Cyclopropanations with [1.1.1]PropellaneDecarboxylative Conjunctive Cross-coupling of Vinyl Boronic Esters using Metallaphotoredox Catalysis1,3-Difunctionalizations of [1.1.1]Propellane via 1,2-Metallate Rearrangements of Boronate ComplexesVisible-Light-Driven Strain-Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters1,2-Boron Shifts of β-Boryl Radicals Generated from Bis-boronic Esters Using Photoredox Catalysis
P50
Q38086592-2641EC0A-C1B0-4D69-AB8E-C8D65C9CED8BQ39397811-0395AAD2-309F-46C6-B53E-D2BF65188D82Q40812313-24CF8C75-5F5A-4209-B734-230A58DCBC9EQ40950916-E66F4976-2BE5-49EE-A314-0F9C5BED4195Q42191984-B83904CC-FE4F-405B-900D-149F22FE2F61Q43121523-D2E52BF6-7101-4187-8CF0-C29075113A63Q46266930-9900067C-7D0C-4CAB-9F45-D6A95CC90F95Q48280572-4912BC8A-79EF-447D-9B18-5AF06651C434Q50143520-6AEF8331-14A8-4DD6-BB95-B66BD8F3797BQ53546286-7174671A-460E-4FA2-87D6-4D0B7CCA342FQ55262275-97C1AD88-A231-4712-B6BB-FA8BA27C7B20Q55617343-6C047930-D970-4018-8A46-C69EA46CA1F3Q56984934-1B3FD0D6-7165-4458-A655-85EAC96E1245Q60029846-BBB6E4C7-9CFA-4F10-9B82-FB0343EB39A8Q60029849-35A3F6D9-EFDE-4C1C-8594-DB1E3539A94CQ60029854-97BDDC45-8A0C-4DB0-B5FC-B5B6D6777CE2Q60029856-34A88D23-2C75-4FC4-B893-0DC77F7A6E75Q60029862-789E0A93-823D-4161-9779-A897BAB54FCDQ60029868-DDF6BABB-150E-446A-B147-FAB04A50A31AQ60029886-5101E6AB-839D-4E6B-9F61-0AA75C2C4A5BQ60029891-3F2A36A6-30FA-422C-A220-8289AE745AC6Q60029893-CA49DBFB-F092-4993-A696-B392BFE2AAFAQ60301047-F899F44E-B9BB-4EEB-A462-495ECC297A5DQ60301051-934D7C4A-EF71-4D6E-8751-DC75FD12186BQ60301056-B4F98053-9F4F-4789-BF8D-233AF2754145Q64091732-84AC782E-D79F-4F86-9AF4-199E3EBF7581Q64237839-D6B40380-4CFD-41F3-865E-D1442113C1EBQ84687503-EE175EC9-3E55-4AA5-9156-ADE96DD59571Q89936227-15E13460-CC57-4FEB-A0AE-5EF719F37FF3Q91226734-DA21166A-0622-466A-9D00-69769987FD0EQ91576854-DF38C3E9-2F62-48A6-8E2D-939A22BC5119Q92469782-51DCD719-4AD0-4ED9-87C1-A11290CE0D3CQ92489209-7C94D7F0-43EA-4E46-8004-3DD94641D9DCQ92489380-3ECF4DA4-6F98-4287-9DD0-483B14A75141Q92957506-31B3DF04-67B6-4514-945D-C2C14D379C72
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Adam Noble
@ast
Adam Noble
@en
Adam Noble
@es
Adam Noble
@nl
Adam Noble
@sl
type
label
Adam Noble
@ast
Adam Noble
@en
Adam Noble
@es
Adam Noble
@nl
Adam Noble
@sl
prefLabel
Adam Noble
@ast
Adam Noble
@en
Adam Noble
@es
Adam Noble
@nl
Adam Noble
@sl
P106
P21
P31
P496
0000-0001-9203-7828