Detalhe da pesquisa
1.
Synthesis of Chiral 1,2-Amino Alcohol-Containing Compounds Utilizing Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Unprotected α-Ketoamines.
J Org Chem
; 89(9): 6085-6099, 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38648720
2.
DFT investigation of coupling constant anomalies in substituted ß-lactams.
Magn Reson Chem
; 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38511664
3.
A Practical Method for the Large-Scale Preparation of the P-Chiral Dihydrobenzoazaphosphole Core by Chemical Resolution.
J Org Chem
; 87(16): 11218-11221, 2022 08 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35930810
4.
Atom-Economical Cross-Coupling of Internal and Terminal Alkynes to Access 1,3-Enynes.
J Am Chem Soc
; 143(10): 3881-3888, 2021 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33683868
5.
A Noncoordinating Acid-Base Catalyst for the Mild and Nonreversible tert-Butylation of Alcohols and Phenols.
J Org Chem
; 86(6): 4877-4882, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33686865
6.
P-Chiral Phosphorus Ligands Based on a 2,3-Dihydrobenzo[ d][1,3]oxaphosphole Motif for Asymmetric Catalysis.
Acc Chem Res
; 52(4): 1101-1112, 2019 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30848882
7.
Nickel-Catalyzed Cross-Electrophile Reductive Couplings of Neopentyl Bromides with Aryl Bromides.
J Org Chem
; 85(12): 8214-8220, 2020 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32452201
8.
Sulfone-Mediated SNAr Reaction as a Powerful Tool for the Synthesis of 4-Quinolinyl Ethers and More-Application to the Synthesis of HCV NS3/4a Protease Inhibitor BI 201420.
J Org Chem
; 85(13): 8339-8351, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32462862
9.
Enantioselective Synthesis of 4-Methyl-3,4-dihydroisocoumarin via Asymmetric Hydroformylation of Styrene Derivatives.
J Org Chem
; 84(8): 4915-4920, 2019 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-30779574
10.
Asymmetric Library Synthesis of P-Chiral t-Butyl-Substituted Secondary and Tertiary Phosphine Oxides.
J Org Chem
; 84(11): 7291-7302, 2019 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31099249
11.
Application of a Preformed Pd-BIDIME Precatalyst to Suzuki-Miyaura Cross-Coupling Reaction in Flow.
J Org Chem
; 84(8): 4926-4931, 2019 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-30715884
12.
Synthesis of highly potent lymphocyte function-associated antigen-1 antagonists labeled with carbon-14 and with stable isotopes, part 3.
J Labelled Comp Radiopharm
; 62(2): 77-85, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30466143
13.
Ligand-Enabled γ-C(sp3)-H Activation of Ketones.
J Am Chem Soc
; 140(10): 3564-3568, 2018 03 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-29481072
14.
Development of a Scalable, Chromatography-Free Synthesis of t-Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3-Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation.
J Org Chem
; 83(3): 1448-1461, 2018 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29323903
15.
Potent and selective CC chemokine receptor 1 antagonists labeled with carbon-13, carbon-14, and tritium.
J Labelled Comp Radiopharm
; 2018 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29766547
16.
Versatile Alkylation of (Hetero)Aryl Iodides with Ketones via ß-C(sp3)-H Activation.
J Am Chem Soc
; 139(45): 16080-16083, 2017 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29086554
17.
Ligand-Enabled Pd(II)-Catalyzed Bromination and Iodination of C(sp3)-H Bonds.
J Am Chem Soc
; 139(16): 5724-5727, 2017 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391681
18.
1,4-Dicarbofunctionalization of 4-Fluoroaryl Grignard and Lithium Reagents with Disubstituted Malononitriles.
J Org Chem
; 82(9): 4993-4997, 2017 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28402664
19.
Synthesis of P-Chiral Dihydrobenzooxaphosphole Core for BI Ligands in Asymmetric Transformations.
J Org Chem
; 82(10): 5456-5460, 2017 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28459568
20.
Development of a 13C NMR Chemical Shift Prediction Procedure Using B3LYP/cc-pVDZ and Empirically Derived Systematic Error Correction Terms: A Computational Small Molecule Structure Elucidation Method.
J Org Chem
; 82(10): 5135-5145, 2017 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28398046