NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids.
about
Nickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates.Highly reactive, single-component nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides.A multiligand based Pd catalyst for C-N cross-coupling reactions.Cross-coupling of mesylated phenol derivatives with potassium ammonio- and amidomethyltrifluoroboratesNickel-catalyzed cross-couplings involving carbon-oxygen bondsCross-Coupling Reactions of Alkenylsilanols with Fluoroalkylsulfonates: Development and Optimization of a Mild and Stereospecific Coupling ProcessIron-catalyzed alkylations of aryl sulfamates and carbamates.Nanonickel-catalyzed Suzuki-Miyaura cross-couplings in water.Methyl 3',5'-dimeth-oxy-biphenyl-4-carboxyl-ate.Methyl 3',4',5'-trimeth-oxy-biphenyl-4-carboxyl-ateA Transmetalation Reaction Enables the Synthesis of [18F]5-Fluorouracil from [18F]Fluoride for Human PET Imaging3,4-Dimeth-oxy-4'-methyl-biphen-yl.A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides.Activation of "inert" alkenyl/aryl C-O bond and its application in cross-coupling reactions.Palladium-catalyzed cross-coupling reactions of aryl mesylates.Triphenylphosphine as a ligand for room-temperature Ni(0)-catalyzed cross-coupling reactions of aryl chlorides with arylboronic acids.Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species.An efficient palladium-benzimidazolyl phosphine complex for the Suzuki-Miyaura coupling of aryl mesylates: facile ligand synthesis and metal complex characterization.Nickel-catalyzed C-P coupling of aryl mesylates and tosylates with H(O)PR1R2.A Highly Practical and Reliable Nickel Catalyst for Suzuki-Miyaura Coupling of Aryl Halides
P2860
Q30496551-63EFB10C-4109-4310-92C3-18AD65726A79Q34310514-50A24C82-D0BD-4419-90D5-5781BCC604CFQ34369527-B2AC8491-9276-4307-A9D1-8AB180F4BE47Q34609427-CF22B2A3-B8AA-452F-B0CB-81D29409D676Q34663409-228928DC-B1F9-4383-ACE7-7B15839C1946Q34812958-DF57E5D1-FFD9-4C12-AACF-F1B03066826CQ36341941-8624E5AD-856F-492A-B604-B222DEED7B8CQ36368093-6B8B03A4-625C-4C6D-8B65-664C367D83DCQ36657137-249C398F-2D95-4CB2-933F-5C0C685AA3F6Q36657285-65893FC1-9A77-4C87-B985-A0947953E379Q36793355-69CC1873-DABA-4189-B2AA-67F6E5DDC3F3Q36826603-E8A691E9-8BB3-47B3-9F90-C9DDBA9DFF8CQ37356701-27A4A021-F5CA-495E-B8A5-B3EA55469BB7Q37833010-776F3AB4-9585-46D3-A36B-2325A39BC047Q37920737-70D58A6E-7E86-47AD-8DF2-3A8C558B505FQ42430155-945B357E-52FD-4D3C-B8F7-B6740C955084Q46441169-96272661-1589-414F-BBEA-1243F0D87886Q52732820-1DF27DE5-4586-4612-A29A-4FC5107D77E6Q54558802-7F73B450-48AC-401B-A826-24F00127DB6BQ56482600-B3B3E1CA-FD60-4AB4-A93C-ABA418E29E90
P2860
NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@en
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@nl
type
label
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@en
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@nl
prefLabel
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@en
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@nl
P2093
P356
P1476
NiCl(2)(dppe)-catalyzed cross- ...... alides with arylboronic acids.
@en
P2093
Geoffrey M Golding
Jan Smidrkal
Oliver Weichold
Virgil Percec
P304
P356
10.1021/JO049940I
P407
P577
2004-05-01T00:00:00Z