Highly Efficient C-SeCF3 Coupling of Aryl Iodides Enabled by an Air-Stable Dinuclear Pd(I) Catalyst.
about
Divergent Reactivity of a Dinuclear (NHC)Nickel(I) Catalyst versus Nickel(0) Enables Chemoselective Trifluoromethylselenolation.Dinuclear Pd(I) complexes with bridging allyl and related ligands.Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air.Rapid Room-Temperature, Chemoselective Csp2 -Csp2 Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air.Nickel-catalyzed trifluoromethylthiolation of Csp2-O bonds.Detection of Palladium(I) in Aerobic Oxidation Catalysis.Synthetic Approaches to Trifluoromethylselenolated Compounds.Trifluoromethylthiolation and Trifluoromethylselenolation of α-Diazo Esters Catalyzed by Copper.Trifluoromethyl- and Fluoroalkylselenolations of Alkynyl Copper(I) Compounds.Dinuclear Nickel(I) and Palladium(I) Complexes for Highly Active Transformations of Organic Compounds.Exploring the Reactivity of Trifluoromethyl Tolueneselenosulfonate with Alkynes under Copper Catalysis.Electrophilic Trifluoromethylselenolation of Boronic Acids.Efficient Synthesis of Trifluoromethyl Amines through a Formal Umpolung Strategy from the Bench-Stable Precursor (Me4 N)SCF3.Expeditious trifluoromethylthiolation and trifluoromethylselenolation of alkynyl(phenyl)iodoniums by [XCF3]- (X = S, Se) anions.Ex situ generation of stoichiometric HCN and its application in the Pd-catalysed cyanation of aryl bromides: evidence for a transmetallation step between two oxidative addition Pd-complexes.Bimetallic catalysis for C-C and C-X coupling reactions.
P2860
Q38631011-C136BEE0-7711-43C0-86AD-A80329CA4F69Q38799784-F36E42DF-87CE-414B-8D92-E696916360CFQ41019125-791861D2-BA57-440D-9701-2F7A557766A9Q41841800-A5B137E7-63FB-4EE2-B1F0-AF0F78E3C262Q42705550-1377AF79-B486-4CEC-9C44-D102424B21FBQ46415270-FFB71DC4-C546-4652-A76B-C01B4189CFDDQ48125283-F75E1848-8D98-4412-8E47-4F87FD8F8D9DQ48174732-0F3CA76C-E7E5-4ABF-8BA4-28C560ECDCB3Q48247384-2D325BBB-BB79-4576-9083-E123064D9D93Q48260373-6B02CAB5-993C-4060-8063-EB0B426CB0FFQ48274186-3DEC632F-24FD-4541-A6D0-9149EE0B70B2Q48797062-34261C44-3C32-4547-8294-56A372B082E3Q48907584-E9A14632-2AE6-4E3A-BFA2-EF6ABA6C1058Q51093164-86D8EC70-D039-4C5F-8230-8CCD79FA24BAQ52345388-A6952A23-C7CF-4148-AE5B-165CFCA32296Q55282835-11169AEE-861F-4C32-BC20-139588E6F899
P2860
Highly Efficient C-SeCF3 Coupling of Aryl Iodides Enabled by an Air-Stable Dinuclear Pd(I) Catalyst.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Highly Efficient C-SeCF3 Coupl ...... able Dinuclear Pd(I) Catalyst.
@en
type
label
Highly Efficient C-SeCF3 Coupl ...... able Dinuclear Pd(I) Catalyst.
@en
prefLabel
Highly Efficient C-SeCF3 Coupl ...... able Dinuclear Pd(I) Catalyst.
@en
P2860
P356
P1476
Highly Efficient C-SeCF3 Coupl ...... able Dinuclear Pd(I) Catalyst.
@en
P2093
Althea S-K Tsang
Marialuisa Aufiero
P2860
P304
10322-10326
P356
10.1002/ANIE.201503388
P407
P577
2015-06-26T00:00:00Z