Phosphinite- and phosphite-based type I palladacycles as highly active catalysts for addition reactions of arylboronic acids with aldehydes, α,β-unsaturated ketones, α-ketoesters, and aldimines

Ping He; Yong Lu; Qiao-Sheng Hu

doi:10.1016/j.tetlet.2007.05.119

Phosphinite- and phosphite-based type I palladacycles as highly active catalysts for addition reactions of arylboronic acids with aldehydes, α,β-unsaturated ketones, α-ketoesters, and aldimines

Tetrahedron Letters ◽

10.1016/j.tetlet.2007.05.119 ◽

2007 ◽

Vol 48 (30) ◽

pp. 5283-5288 ◽

Cited By ~ 68

Author(s):

Ping He ◽

Yong Lu ◽

Qiao-Sheng Hu

Keyword(s):

Addition Reactions ◽

Type I ◽

Unsaturated Ketones ◽

Arylboronic Acids ◽

Highly Active

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Phosphinite- and Phosphite-Based Type I Palladacycles as Highly Active Catalysts for Addition Reactions of Arylboronic Acids with Aldehydes, α,β-Unsaturated Ketones, α-Ketoesters, and Aldimines.

ChemInform ◽

10.1002/chin.200745088 ◽

2007 ◽

Vol 38 (45) ◽

Author(s):

Ping He ◽

Yong Lu ◽

Qiao-Sheng Hu

Keyword(s):

Addition Reactions ◽

Type I ◽

Unsaturated Ketones ◽

Arylboronic Acids ◽

Highly Active

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Anionic Four-Electron Donor-Based Palladacycles as Catalysts for Addition Reactions of Arylboronic Acids with α,β-Unsaturated Ketones, Aldehydes, and α-Ketoesters

Organic Letters ◽

10.1021/ol062814b ◽

2007 ◽

Vol 9 (2) ◽

pp. 343-346 ◽

Cited By ~ 115

Author(s):

Ping He ◽

Yong Lu ◽

Cheng-Guo Dong ◽

Qiao-Sheng Hu

Keyword(s):

Electron Donor ◽

Addition Reactions ◽

Unsaturated Ketones ◽

Arylboronic Acids

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Anionic Four-Electron Donor-Based Palladacycles as Catalysts for Addition Reactions of Arylboronic Acids with α,β-Unsaturated Ketones, Aldehydes, and α-Ketoesters.

ChemInform ◽

10.1002/chin.200720086 ◽

2007 ◽

Vol 38 (20) ◽

Author(s):

Ping He ◽

Yong Lu ◽

Cheng-Guo Dong ◽

Qiao-Sheng Hu

Keyword(s):

Electron Donor ◽

Addition Reactions ◽

Unsaturated Ketones ◽

Arylboronic Acids

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Highly enantioselective aza-Michael addition reactions of 4-nitrophthalimide with α,β-unsaturated ketones

RSC Advances ◽

10.1039/c3ra41179f ◽

2013 ◽

Vol 3 (29) ◽

pp. 11498 ◽

Cited By ~ 7

Author(s):

Shijun Ma ◽

Lulu Wu ◽

Ming Liu ◽

Xiufang Xu ◽

Yaodong Huang ◽

...

Keyword(s):

Michael Addition ◽

Addition Reactions ◽

Unsaturated Ketones

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ChemInform Abstract: Enantioselective Synthesis of α-Aryl Alkylamines by Rh-Catalyzed Addition Reactions of Arylboronic Acids to Aliphatic Imines.

ChemInform ◽

10.1002/chin.200847075 ◽

2008 ◽

Vol 39 (47) ◽

Author(s):

Monica Trincado ◽

Jonathan A. Ellman

Keyword(s):

Enantioselective Synthesis ◽

Addition Reactions ◽

Arylboronic Acids

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Theoretical studies of ruthenium hydride-catalyzed addition reactions of benzaldehydes to isoprenes leading to β,γ-unsaturated ketones: The role of the ligands hydride, carbonyl, chloride, and triphenylphosphine of the catalyst

Journal of Organometallic Chemistry ◽

10.1016/j.jorganchem.2013.12.012 ◽

2014 ◽

Vol 753 ◽

pp. 1-8 ◽

Cited By ~ 6

Author(s):

Fen Wang ◽

Qingxi Meng ◽

Ming Li

Keyword(s):

Addition Reactions ◽

Theoretical Studies ◽

Ruthenium Hydride ◽

Unsaturated Ketones ◽

Carbonyl Chloride

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ChemInform Abstract: NOTE ON THE DIRECT α-PHENYLSULFENYLATION OF ENOLATES GENERATED DURING 1,4-ADDITION REACTIONS ON α,β-UNSATURATED KETONES

Chemischer Informationsdienst ◽

10.1002/chin.197730127 ◽

1977 ◽

Vol 8 (30) ◽

pp. no-no

Author(s):

M. SAMSON ◽

H. DE WILDE ◽

M. VANDEWALLE

Keyword(s):

Addition Reactions ◽

Unsaturated Ketones

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Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media

Tetrahedron Letters ◽

10.1016/j.tetlet.2016.12.071 ◽

2017 ◽

Vol 58 (8) ◽

pp. 726-731 ◽

Cited By ~ 18

Author(s):

Guiyan Liu ◽

Chengxin Liu ◽

Fangwai Han ◽

Zhongliang Wang ◽

Jianhui Wang

Keyword(s):

Palladium Catalysts ◽

Room Temperature ◽

Aqueous Media ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Arylboronic Acids ◽

Highly Active

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ChemInform Abstract: ELECTRON TRANSFER IN NICKEL-CATALYZED ADDITION REACTIONS OF ORGANOZIRCONIUM COMPOUNDS TO UNSATURATED KETONES

Chemischer Informationsdienst ◽

10.1002/chin.198144263 ◽

1981 ◽

Vol 12 (44) ◽

Author(s):

F. M. DAYRIT ◽

J. SCHWARTZ

Keyword(s):

Electron Transfer ◽

Addition Reactions ◽

Unsaturated Ketones ◽

Organozirconium Compounds

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ChemInform Abstract: Well-Defined [Rh(NHC)(OH)] Complexes Enabling the Conjugate Addition of Arylboronic Acids to α,β-Unsaturated Ketones.

ChemInform ◽

10.1002/chin.201212082 ◽

2012 ◽

Vol 43 (12) ◽

pp. no-no

Author(s):

Byron J. Truscott ◽

George C. Fortman ◽

Alexandra M. Z. Slawin ◽

Steven P. Nolan

Keyword(s):

Conjugate Addition ◽

Unsaturated Ketones ◽

Arylboronic Acids

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