Detalhe da pesquisa
1.
Amine-Functionalized Polybutadiene Synthesis by Tunable Postpolymerization Hydroaminoalkylation.
J Am Chem Soc
; 145(42): 22871-22877, 2023 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37819801
2.
One-Pot Sequential Hydroamination Protocol for N-Heterocycle Synthesis: One Method To Access Five Different Classes of Tri-Substituted Pyridines.
J Org Chem
; 88(3): 1378-1384, 2023 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36634317
3.
Hydroaminoalkylation for the Catalytic Addition of Amines to Alkenes or Alkynes: Diverse Mechanisms Enable Diverse Substrate Scope.
J Am Chem Soc
; 144(26): 11459-11481, 2022 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35731810
4.
Direct, Catalytic α-Alkylation of N-Heterocycles by Hydroaminoalkylation: Substrate Effects for Regiodivergent Product Formation.
J Am Chem Soc
; 143(29): 11243-11250, 2021 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34278789
5.
Zirconium Catalyzed Hydroaminoalkylation for the Synthesis of α-Arylated Amines and N-Heterocycles.
Chemistry
; 27(20): 6334-6339, 2021 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33427338
6.
Titanium catalysis for the synthesis of fine chemicals - development and trends.
Chem Soc Rev
; 49(19): 6947-6994, 2020 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32852007
7.
Zirconium-Catalyzed Hydroaminoalkylation of Alkynes for the Synthesis of Allylic Amines.
J Am Chem Soc
; 142(49): 20566-20571, 2020 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33249842
8.
Cyclic Ureate Tantalum Catalyst for Preferential Hydroaminoalkylation with Aliphatic Amines: Mechanistic Insights into Substrate Controlled Reactivity.
J Am Chem Soc
; 142(37): 15740-15750, 2020 09 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32786765
9.
Vanadium Pyridonate Catalysts: Isolation of Intermediates in the Reductive Coupling of Alcohols.
Inorg Chem
; 59(8): 5256-5260, 2020 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32223129
10.
Zirconium Hydroaminoalkylation. An Alternative Disconnection for the Catalytic Synthesis of α-Arylated Primary Amines.
J Am Chem Soc
; 141(48): 18944-18948, 2019 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31718171
11.
Regio- and Stereoselective Hydroamination of Alkynes Using an Ammonia Surrogate: Synthesis of N-Silylenamines as Reactive Synthons.
J Am Chem Soc
; 140(15): 4973-4976, 2018 04 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29528631
12.
Understanding Ni(II)-Mediated C(sp3)-H Activation: Tertiary Ureas as Model Substrates.
J Am Chem Soc
; 140(39): 12602-12610, 2018 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30185028
13.
Ti-Catalyzed Hydroamination for the Synthesis of Amine-Containing π-Conjugated Materials.
Chemistry
; 24(21): 5562-5568, 2018 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29282775
14.
1,3-N,O-Complexes of late transition metals. Ligands with flexible bonding modes and reaction profiles.
Chem Soc Rev
; 46(10): 2913-2940, 2017 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-28426030
15.
Catalytic and Atom-Economic Csp3 -Csp3 Bond Formation: Alkyl Tantalum Ureates for Hydroaminoalkylation.
Angew Chem Int Ed Engl
; 57(13): 3469-3472, 2018 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29330909
16.
Bis(tert-butylimido)bis(N,O-chelate)tungsten(VI) Complexes: Probing Amidate and Pyridonate Hemilability.
Inorg Chem
; 56(10): 5553-5566, 2017 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28443662
17.
Toward anti-Markovnikov 1-Alkyne O-Phosphoramidation: Exploiting Metal-Ligand Cooperativity in a 1,3-N,O-Chelated Cp*Ir(III) Complex.
J Am Chem Soc
; 138(27): 8396-9, 2016 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27327491
18.
N,O-Chelating Four-Membered Metallacyclic Titanium(IV) Complexes for Atom-Economic Catalytic Reactions.
Acc Chem Res
; 48(9): 2576-86, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26247696
19.
Phosphoramidate-Supported Cp*Ir(III) Aminoborane H2 B=NR2 Complexes: Synthesis, Structure, and Solution Dynamics.
Chemistry
; 22(20): 6793-7, 2016 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26946099
20.
Catalytic Asymmetric Synthesis of Morpholines. Using Mechanistic Insights To Realize the Enantioselective Synthesis of Piperazines.
J Org Chem
; 81(19): 8696-8709, 2016 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27668321