Detalhe da pesquisa
1.
Nickel-Catalyzed Reductive [4 + 1] Sila-Cycloaddition of 1,3-Dienes with Dichlorosilanes.
J Am Chem Soc
; 145(24): 13008-13014, 2023 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37285283
2.
Reductive Cross-Coupling of Unreactive Electrophiles.
Acc Chem Res
; 55(17): 2491-2509, 2022 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35951536
3.
Nickel-Catalyzed Reductive Coupling of Chlorosilanes.
Chemistry
; 29(11): e202203362, 2023 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36426828
4.
Nickel-Catalyzed Cross-Electrophile 1,2-Silyl-Arylation of 1,3-Dienes with Chlorosilanes and Aryl Bromides.
Angew Chem Int Ed Engl
; 62(4): e202215703, 2023 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36428246
5.
Nickel-Catalyzed Reductive C(sp2 )-Si Coupling of Chlorohydrosilanes via Si-Cl Cleavage.
Angew Chem Int Ed Engl
; 61(21): e202200215, 2022 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35263015
6.
Reductive Alkylation of Alkenyl Acetates with Alkyl Bromides by Nickel Catalysis.
Angew Chem Int Ed Engl
; 61(4): e202114556, 2022 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34862693
7.
Cobalt-Catalyzed Enantiospecific Dynamic Kinetic Cross-Electrophile Vinylation of Allylic Alcohols with Vinyl Triflates.
J Am Chem Soc
; 143(39): 15930-15935, 2021 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34570474
8.
Regiocontrolled Reductive Vinylation of Aliphatic 1,3-Dienes with Vinyl Triflates by Nickel Catalysis.
J Am Chem Soc
; 143(12): 4536-4542, 2021 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33724807
9.
Nickel-Catalyzed Reductive C-Ge Coupling of Aryl/Alkenyl Electrophiles with Chlorogermanes.
Angew Chem Int Ed Engl
; 60(51): 26571-26576, 2021 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-34693605
10.
Highly Enantioselective Cross-Electrophile Aryl-Alkenylation of Unactivated Alkenes.
J Am Chem Soc
; 141(18): 7637-7643, 2019 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31002758
11.
Decryption of Active Constituents and Action Mechanism of the Traditional Uighur Prescription (BXXTR) Alleviating IMQ-Induced Psoriasis-Like Skin Inflammation in BALB/c Mice.
Int J Mol Sci
; 19(7)2018 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-29933541
12.
Copper-Catalyzed Tandem Aerobic Oxidative Cyclization for the Synthesis of Polysubstituted Quinolines via C(sp3)/C(sp2)-H Bond Functionalization.
J Org Chem
; 82(19): 10110-10120, 2017 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28929749
13.
tert-Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied.
Org Biomol Chem
; 15(30): 6318-6322, 2017 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28730188
14.
Iodine-mediated thiolation of substituted naphthols/naphthylamines and arylsulfonyl hydrazides via C(sp2)-H bond functionalization.
J Org Chem
; 79(21): 10605-10, 2014 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25322279
15.
Nickel-Catalyzed Reductive Csp3-Ge Coupling of Alkyl Bromides with Chlorogermanes.
Org Lett
; 24(9): 1802-1806, 2022 03 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35209712
16.
Nickel-Catalyzed Cross-Electrophile C(sp3)-Si Coupling of Unactivated Alkyl Bromides with Vinyl Chlorosilanes.
Org Lett
; 23(20): 7855-7859, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34608801
17.
Analyses and identification of the chemical constituents of the Uighur formulation Baixuan Xiatare using three-stage infrared spectroscopy.
J Tradit Chin Med
; 40(5): 875-882, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33000590
18.
Ni-catalyzed cross-electrophile coupling between vinyl/aryl and alkyl sulfonates: synthesis of cycloalkenes and modification of peptides.
Chem Sci
; 10(37): 8706-8712, 2019 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31803446
19.
Commonalities and characteristics of aqueous extracts from three Uighur medicines were analyzed by using three-stage infrared spectroscopy combined with ultra-performance liquid chromatography-time of flight-mass spectra.
J Tradit Chin Med
; 39(1): 118-126, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32186032
20.
I2-catalyzed synthesis of substituted imidazoles from vinyl azides and benzylamines.
Chem Commun (Camb)
; 51(30): 6598-600, 2015 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25775109