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Palladium(II)-Catalyzed Enantioselective C(sp3)–H Activation Using a Chiral Hydroxamic Acid Ligand
Palladium(II)-Catalyzed Enantioselective C(sp3)–H Activation Using a Chiral Hydroxamic Acid Ligand
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Palladium(II)-Catalyzed Enantioselective C(sp3)–H Activation Using a Chiral Hydroxamic Acid Ligand

Xiao, Kai-Jiong ; Lin, David W ; Miura, Motofumi ; Zhu, Ru-Yi ; Gong, Wei ; Wasa, Masayuki ; Yu, Jin-Quan

Journal of the American Chemical Society, 2014-06, Vol.136 (22), p.8138-8142 [Periódico revisado por pares]

United States: American Chemical Society

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2
Direct Transformation of Secondary Amides into Secondary Amines: Triflic Anhydride Activated Reductive Alkylation
Direct Transformation of Secondary Amides into Secondary Amines: Triflic Anhydride Activated Reductive Alkylation
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Direct Transformation of Secondary Amides into Secondary Amines: Triflic Anhydride Activated Reductive Alkylation

Xiao, Kai-Jiong ; Wang, Ai-E ; Huang, Pei-Qiang

Angewandte Chemie (International ed.), 2012-08, Vol.51 (33), p.8314-8317 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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3
Direct, One-pot Sequential Reductive Alkylation of Lactams/Amides with Grignard and Organolithium Reagents through Lactam/Amide Activation
Direct, One-pot Sequential Reductive Alkylation of Lactams/Amides with Grignard and Organolithium Reagents through Lactam/Amide Activation
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Direct, One-pot Sequential Reductive Alkylation of Lactams/Amides with Grignard and Organolithium Reagents through Lactam/Amide Activation

Xiao, Kai-Jiong ; Luo, Jie-Min ; Ye, Ke-Yin ; Wang, Yu ; Huang, Pei-Qiang

Angewandte Chemie (International ed.), 2010-04, Vol.49 (17), p.3037-3040 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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4
Ligand-Enabled Arylation of γ-C−H Bonds
Ligand-Enabled Arylation of γ-C−H Bonds
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Ligand-Enabled Arylation of γ-C−H Bonds

Li, Suhua ; Zhu, Ru-Yi ; Xiao, Kai-Jiong ; Yu, Jin-Quan

Angewandte Chemie (International ed.), 2016-03, Vol.55 (13), p.4317-4321 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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5
Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones
Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones
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Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones

Huang, Pei-Qiang ; Ou, Wei ; Xiao, Kai-Jiong ; Wang, Ai-E

Chemical communications (Cambridge, England), 2014-08, Vol.50 (63), p.8761-8763 [Periódico revisado por pares]

England

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6
A general method for the direct transformation of common tertiary amides into ketones and amines by addition of Grignard reagents
A general method for the direct transformation of common tertiary amides into ketones and amines by addition of Grignard reagents
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A general method for the direct transformation of common tertiary amides into ketones and amines by addition of Grignard reagents

Huang, Pei-Qiang ; Wang, Yu ; Xiao, Kai-Jiong ; Huang, Ying-Hong

Tetrahedron, 2015-06, Vol.71 (24), p.4248-4254 [Periódico revisado por pares]

Elsevier Ltd

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7
Versatile One-Pot Reductive Alkylation of Lactams/Amides via Amide Activation: Application to the Concise Syntheses of Bioactive Alkaloids (±)-Bgugaine, (±)-Coniine, (+)-Preussin, and (−)-Cassine
Versatile One-Pot Reductive Alkylation of Lactams/Amides via Amide Activation: Application to the Concise Syntheses of Bioactive Alkaloids (±)-Bgugaine, (±)-Coniine, (+)-Preussin, and (−)-Cassine
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Versatile One-Pot Reductive Alkylation of Lactams/Amides via Amide Activation: Application to the Concise Syntheses of Bioactive Alkaloids (±)-Bgugaine, (±)-Coniine, (+)-Preussin, and (−)-Cassine

Xiao, Kai-Jiong ; Wang, Yu ; Ye, Ke-Yin ; Huang, Pei-Qiang

Chemistry : a European journal, 2010-11, Vol.16 (43), p.12792-12796 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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8
Ligand-Enabled Arylation of [gamma]-C-H Bonds
Ligand-Enabled Arylation of [gamma]-C-H Bonds
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Ligand-Enabled Arylation of [gamma]-C-H Bonds

Li, Suhua ; Zhu, Ru-Yi ; Xiao, Kai-Jiong ; Yu, Jin-Quan

Angewandte Chemie (International ed.), 2016-03, Vol.55 (13), p.4317 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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9
General One-Pot Reductive gem-Bis-Alkylation of Tertiary Lactams/Amides: Rapid Construction of 1-Azaspirocycles and Formal Total Synthesis of (±)-Cephalotaxine
General One-Pot Reductive gem-Bis-Alkylation of Tertiary Lactams/Amides: Rapid Construction of 1-Azaspirocycles and Formal Total Synthesis of (±)-Cephalotaxine
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General One-Pot Reductive gem-Bis-Alkylation of Tertiary Lactams/Amides: Rapid Construction of 1-Azaspirocycles and Formal Total Synthesis of (±)-Cephalotaxine

Xiao, Kai-Jiong ; Luo, Jie-Min ; Xia, Xiao-Er ; Wang, Yu ; Huang, Pei-Qiang

Chemistry : a European journal, 2013-09, Vol.19 (39), p.13075-13086 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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10
A Direct and General Method for the Reductive Alkylation of Tertiary Lactams/Amides: Application to the Step Economical Synthesis of Alkaloid (−)-Morusimic Acid D
A Direct and General Method for the Reductive Alkylation of Tertiary Lactams/Amides: Application to the Step Economical Synthesis of Alkaloid (−)-Morusimic Acid D
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A Direct and General Method for the Reductive Alkylation of Tertiary Lactams/Amides: Application to the Step Economical Synthesis of Alkaloid (−)-Morusimic Acid D

Xiao, Kai-Jiong ; Wang, Yu ; Huang, Ying-Hong ; Wang, Xiao-Gang ; Huang, Pei-Qiang

Journal of organic chemistry, 2013-09, Vol.78 (17), p.8305-8311 [Periódico revisado por pares]

United States: American Chemical Society

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