about
Enantioselective protonation.Catalytic enantioselective stereoablative reactions: an unexploited approach to enantioselective catalysisAnesthetic potency of two novel synthetic polyhydric alkanols longer than the n-alkanol cutoff: evidence for a bilayer-mediated mechanism of anesthesia?Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation.Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition.Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Cyclopentanones.Enantioselective Tsuji allylations.Natural products as inspiration for the development of asymmetric catalysis.Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.Homogeneous pd-catalyzed enantioselective decarboxylative protonation.The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation.Enantioselective total synthesis of (+)-cassiol.The inner-sphere process in the enantioselective Tsuji allylation reaction with (S)-t-Bu-phosphinooxazoline ligands.Catalytic enantioselective decarboxylative protonation.Deracemization of quaternary stereocenters by Pd-catalyzed enantioconvergent decarboxylative allylation of racemic beta-ketoesters.Cascade Mn-Mediated γ-Alkylation/oxa-Michael Addition of Enones with 1,3-Dicarbonyls.Regiocontrolled Oxidative C-C Coupling of Dienol Ethers and 1,3-Dicarbonyl Compounds.Regiodivergent halogenation of vinylogous esters: one-pot, transition-metal-free access to differentiated haloresorcinols.Short Enantioselective Formal Synthesis of (–)-PlatencinCu-Catalyzed Stereoselective γ-Alkylation of EnonesDirect Regioselective γ-Amination of EnonesCopper-Catalyzed γ-Sulfonylation of α,β-Unsaturated Carbonyl Compounds by Means of Silyl Dienol Ethers
P50
Q33812467-54D73A90-9E36-44FD-B76D-E1B504C08CB9Q34236967-76670754-792B-4EEC-882A-24600B951AB1Q34424784-A844F948-DB92-490F-88EE-DAF20F7594E9Q34462839-FC60FBFA-EBBB-45B0-8BE2-1A207DA5BEA4Q35889116-103DB565-E664-4183-A939-0EB13F70AD5BQ36267155-0D1363F0-011D-4598-A8F4-94269ACD3577Q36970379-BA53F33C-5467-4E8F-B6A1-896B470C8F53Q37272545-43172869-7261-446D-96B1-8C307EE567BDQ42182848-C58BFCA1-7D06-4528-B62C-47ED3D127A13Q42394240-50A4CFAE-BE3F-417B-A028-DBAF8A8E554AQ42534222-6F9CA6B4-5FDB-435A-8791-ADA658151FCDQ43098590-AF2C33FD-0F6F-4F52-BDE8-AECF7DE84FAEQ45962583-2883C029-83A2-4766-867D-A1B4890ECE04Q45999784-EC64A100-C89B-4983-BA92-702BAB655640Q46249389-10927F0C-1456-410D-94DA-D143F12358D5Q48278114-AA3EE123-CF60-44A6-829D-F1682CED0045Q50800420-34D9AFE0-CEF5-49CE-9ECC-438669267D75Q51019752-006F304A-F8FC-4E4C-9238-B2EC34826FB1Q59783800-EF9A5993-BCA8-48A2-B9C9-0A7A69D6BC72Q59783805-AA014E6F-2E63-4AA8-9DEA-8C069146395DQ59783806-3A9EA5BF-8F4C-497F-BE63-F29BCE1D598FQ59783807-4ACC16AF-680F-400E-94B4-83F466FD94B5
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Justin T Mohr
@ast
Justin T Mohr
@en
Justin T Mohr
@es
Justin T Mohr
@nl
Justin T Mohr
@sl
type
label
Justin T Mohr
@ast
Justin T Mohr
@en
Justin T Mohr
@es
Justin T Mohr
@nl
Justin T Mohr
@sl
prefLabel
Justin T Mohr
@ast
Justin T Mohr
@en
Justin T Mohr
@es
Justin T Mohr
@nl
Justin T Mohr
@sl
P106
P21
P31
P496
0000-0002-7005-3322