Si−C Bond Activation of ArMe2SiOH Promoted by a Bromoplatinum(II) Complex and Ag2O. Aryl Group Transfer from Silicon to Platinum

Neli Mintcheva; Yasushi Nishihara; Makoto Tanabe; Kazunori Hirabayashi; Atsunori Mori; Kohtaro Osakada

doi:10.1021/om010006c

Si−C Bond Activation of ArMe2SiOH Promoted by a Bromoplatinum(II) Complex and Ag2O. Aryl Group Transfer from Silicon to Platinum

Organometallics ◽

10.1021/om010006c ◽

2001 ◽

Vol 20 (6) ◽

pp. 1243-1246 ◽

Cited By ~ 18

Author(s):

Neli Mintcheva ◽

Yasushi Nishihara ◽

Makoto Tanabe ◽

Kazunori Hirabayashi ◽

Atsunori Mori ◽

...

Keyword(s):

Bond Activation ◽

Aryl Group ◽

Group Transfer

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Gold-Catalyzed C-S Aryl-Group Transfer in Zinc Finger Proteins

Angewandte Chemie ◽

10.1002/ange.201803082 ◽

2018 ◽

Vol 130 (30) ◽

pp. 9449-9453 ◽

Cited By ~ 4

Author(s):

Raphael E. F. de Paiva ◽

Zhifeng Du ◽

Douglas H. Nakahata ◽

Frederico A. Lima ◽

Pedro P. Corbi ◽

...

Keyword(s):

Zinc Finger ◽

Zinc Finger Proteins ◽

Aryl Group ◽

Group Transfer

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Synthesis and protonation of cyclohexadienyl manganese acylmetallates; alkyl and aryl group transfer from an acyl to a dienyl ligand

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39900001226 ◽

1990 ◽

pp. 1226 ◽

Cited By ~ 2

Author(s):

Ranbir S. Padda ◽

John B. Sheridan ◽

Karen Chaffee

Keyword(s):

Aryl Group ◽

Group Transfer

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P−C Bond Activation and Phenyl Group Transfer in the Reaction of Co4(CO)9(mesitylene) with 2,3-Bis(diphenylphosphino)maleic Anhydride (bma). X-ray Diffraction Structures and Redox Properties of Co3(CO)7[μ2-η2,η1-P(Ph)CC(PPh2)C(O)OC(O)] and Co3(CO)6(PPh3)[μ2-η2,η1-P(Ph)CC(PPh2)C(O)OC(O)]

Organometallics ◽

10.1021/om960401g ◽

1996 ◽

Vol 15 (21) ◽

pp. 4480-4487 ◽

Cited By ~ 15

Author(s):

Chun-Gu Xia ◽

Kaiyuan Yang ◽

Simon G. Bott ◽

Michael G. Richmond

Keyword(s):

Maleic Anhydride ◽

Bond Activation ◽

Phenyl Group ◽

Redox Properties ◽

X Ray Diffraction ◽

X Ray ◽

Group Transfer

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Palladium-Catalyzed Aryl Group Transfer from Triarylphosphines to Arylboronic Acids

Polyhedron ◽

10.1016/j.poly.2021.115550 ◽

2021 ◽

pp. 115550

Author(s):

Purna C.R. Vasireddy ◽

Akash R. Gogate ◽

Dale R. Enright ◽

Irina P. Smoliakova

Keyword(s):

Aryl Group ◽

Group Transfer ◽

Arylboronic Acids ◽

Palladium Catalyzed

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Aryl‐Aryl Cross‐Coupling with Hypervalent Iodine Reagents: Aryl Group Transfer Reactions

ChemistrySelect ◽

10.1002/slct.202003396 ◽

2020 ◽

Vol 5 (43) ◽

pp. 13644-13655

Author(s):

Manoj Kumar Ghosh ◽

Nilendri Rout

Keyword(s):

Cross Coupling ◽

Transfer Reactions ◽

Hypervalent Iodine ◽

Aryl Group ◽

Group Transfer

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Direct Exchange of a Ketone Methyl or Aryl Group to Another Aryl Group through CC Bond Activation Assisted by Rhodium Chelation

Angewandte Chemie ◽

10.1002/ange.201206693 ◽

2012 ◽

Vol 124 (49) ◽

pp. 12500-12504 ◽

Cited By ~ 15

Author(s):

Jingjing Wang ◽

Weiqiang Chen ◽

Sujing Zuo ◽

Lu Liu ◽

Xinrui Zhang ◽

...

Keyword(s):

Bond Activation ◽

Aryl Group ◽

Direct Exchange

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A utility for organoleads: selective alkyl and aryl group transfer to tin

Dalton Transactions ◽

10.1039/c7dt04520d ◽

2018 ◽

Vol 47 (5) ◽

pp. 1703-1708 ◽

Cited By ~ 3

Author(s):

Renzo N. Arias-Ugarte ◽

Keith H. Pannell

Keyword(s):

Molar Ratio ◽

Aryl Group ◽

Group Transfer

Me4Pb and Ph4Pb readily transfer methyl or phenyl groups to an equivalent molar ratio of tin(iv) chlorides in the order SnCl4 > MeSnCl3 > Me2SnCl2 > Me3SnCl, often in a selective manner.

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The aryl group transfer process from a triarylphosphine to a chlorotetrakis(amidato)diruthenium(II,III) species: syntheses and molecular structures of Ru2(R)2(R'CONH)2[R2POC(R')N]2 (R = C6H5, R' = 3,5-(OCH3)2C6H3; R = p-C6H4CH3, R' = C6H5)

Inorganic Chemistry ◽

10.1021/ic00216a021 ◽

1985 ◽

Vol 24 (22) ◽

pp. 3584-3589 ◽

Cited By ~ 23

Author(s):

Akhil R. Chakravarty ◽

F. Albert Cotton

Keyword(s):

Transfer Process ◽

Molecular Structures ◽

Aryl Group ◽

Group Transfer

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Benzannulated annulenes. 10. Unusual macrocyclic biphenyls containing the dihydropyrene nucleus. An observation of aryl group transfer from phosphine to aryl halide using nickel complexes

Journal of the American Chemical Society ◽

10.1021/ja00337a021 ◽

1984 ◽

Vol 106 (25) ◽

pp. 7776-7779 ◽

Cited By ~ 17

Author(s):

Reginald H. Mitchell ◽

Mahima Chaudhary ◽

Thomas W. Dingle ◽

Richard Vaughan Williams

Keyword(s):

Aryl Halide ◽

Nickel Complexes ◽

Aryl Group ◽

Group Transfer

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New hydrosilylation reaction of arylacetylene accompanied by C-H bond activation catalyzed by a xantsil ruthenium complex

Pure and Applied Chemistry ◽

10.1351/pac200880051155 ◽

2008 ◽

Vol 80 (5) ◽

pp. 1155-1160 ◽

Cited By ~ 16

Author(s):

Hiromi Tobita ◽

Nobukazu Yamahira ◽

Keisuke Ohta ◽

Takashi Komuro ◽

Masaaki Okazaki

Keyword(s):

Bond Activation ◽

Ruthenium Complex ◽

Phosphine Ligand ◽

The Other ◽

Aryl Group ◽

Hydrosilylation Reaction ◽

New Type ◽

Silyl Complex ◽

Phosphine Complex ◽

Catalytic Hydrosilylation

A new type of catalytic hydrosilylation of arylalkynes was induced by a 16-electron ruthenium bis(silyl) phosphine complex, resulting in ortho-silylation of the aryl group as well as a hydrogenation of the alkyne CC bond to give an (E)-form of alkene selectively. On the other hand, the same reaction using a related bis(silyl) complex having an η6-toluene ligand instead of the phosphine ligand as a catalyst led to a normal hydrosilylation reaction to afford silylalkene.

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