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Efficient and novel one-pot synthesis of polycycles bearing cyclols by FeCl3-promoted [2 + 2] cycloaddition: application to cannabicyclol, cannabicyclovarin, and ranhuadujuanine A
Efficient and novel one-pot synthesis of polycycles bearing cyclols by FeCl3-promoted [2 + 2] cycloaddition: application to cannabicyclol, cannabicyclovarin, and ranhuadujuanine A
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Efficient and novel one-pot synthesis of polycycles bearing cyclols by FeCl3-promoted [2 + 2] cycloaddition: application to cannabicyclol, cannabicyclovarin, and ranhuadujuanine A

Li, Xin ; Lee, Yong Rok

Organic & biomolecular chemistry, 2014-02, Vol.12 (8), p.1250-1257 [Periódico revisado por pares]

England

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2
The application of flow microreactors to the preparation of a family of casein kinase I inhibitors
The application of flow microreactors to the preparation of a family of casein kinase I inhibitors
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The application of flow microreactors to the preparation of a family of casein kinase I inhibitors

Venturoni, Francesco ; Nikbin, Nikzad ; Ley, Steven V ; Baxendale, Ian R

Organic & biomolecular chemistry, 2010-01, Vol.8 (8), p.1798-1806 [Periódico revisado por pares]

England

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3
The use of click chemistry in the emerging field of catalomics
The use of click chemistry in the emerging field of catalomics
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The use of click chemistry in the emerging field of catalomics

Kalesh, Karunakaran A ; Shi, Haibin ; Ge, Jingyan ; Yao, Shao Q

Organic & biomolecular chemistry, 2010-01, Vol.8 (8), p.1749-1762 [Periódico revisado por pares]

England

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4
Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts
Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts
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Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts

Ichiishi, Naoko ; Brooks, Allen F ; Topczewski, Joseph J ; Rodnick, Melissa E ; Sanford, Melanie S ; Scott, Peter J. H

Organic letters, 2014-06, Vol.16 (12), p.3224-3227 [Periódico revisado por pares]

United States: American Chemical Society

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5
Electrophilic Trifluoromethylation by Copper-Catalyzed Addition of CF3-Transfer Reagents to Alkenes and Alkynes
Electrophilic Trifluoromethylation by Copper-Catalyzed Addition of CF3-Transfer Reagents to Alkenes and Alkynes
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Electrophilic Trifluoromethylation by Copper-Catalyzed Addition of CF3-Transfer Reagents to Alkenes and Alkynes

Janson, Pär G ; Ghoneim, Ibrahim ; Ilchenko, Nadia O ; Szabó, Kálmán J

Organic letters, 2012-06, Vol.14 (11), p.2882-2885 [Periódico revisado por pares]

United States: American Chemical Society

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6
Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via C−H Activation
Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via C−H Activation
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Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via C−H Activation

Tsai, Andy S. ; Brasse, Mikaël ; Bergman, Robert G. ; Ellman, Jonathan A.

Organic letters, 2011-02, Vol.13 (3), p.540-542 [Periódico revisado por pares]

United States: American Chemical Society

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7
Highly Practical Synthesis of Nitriles and Heterocycles from Alcohols under Mild Conditions by Aerobic Double Dehydrogenative Catalysis
Highly Practical Synthesis of Nitriles and Heterocycles from Alcohols under Mild Conditions by Aerobic Double Dehydrogenative Catalysis
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Highly Practical Synthesis of Nitriles and Heterocycles from Alcohols under Mild Conditions by Aerobic Double Dehydrogenative Catalysis

Yin, Weiyu ; Wang, Chengming ; Huang, Yong

Organic letters, 2013-04, Vol.15 (8), p.1850-1853 [Periódico revisado por pares]

United States: American Chemical Society

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8
Copper-Catalyzed Domino Synthesis of Quinazolinones via Ullmann-Type Coupling and Aerobic Oxidative C−H Amidation
Copper-Catalyzed Domino Synthesis of Quinazolinones via Ullmann-Type Coupling and Aerobic Oxidative C−H Amidation
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Copper-Catalyzed Domino Synthesis of Quinazolinones via Ullmann-Type Coupling and Aerobic Oxidative C−H Amidation

Xu, Wei ; Jin, Yibao ; Liu, Hongxia ; Jiang, Yuyang ; Fu, and Hua

Organic letters, 2011-03, Vol.13 (6), p.1274-1277 [Periódico revisado por pares]

United States: American Chemical Society

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9
Multicomponent reactions: a sustainable tool to 1,2- and 1,3-azoles
Multicomponent reactions: a sustainable tool to 1,2- and 1,3-azoles
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Multicomponent reactions: a sustainable tool to 1,2- and 1,3-azoles

Preeti ; Singh, Krishna Nand

Organic & biomolecular chemistry, 2018-12, Vol.16 (47), p.984-9116 [Periódico revisado por pares]

England: Royal Society of Chemistry

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10
Mild and Selective Heterogeneous Catalytic Hydration of Nitriles to Amides by Flowing through Manganese Dioxide
Mild and Selective Heterogeneous Catalytic Hydration of Nitriles to Amides by Flowing through Manganese Dioxide
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Mild and Selective Heterogeneous Catalytic Hydration of Nitriles to Amides by Flowing through Manganese Dioxide

Battilocchio, Claudio ; Hawkins, Joel M ; Ley, Steven V

Organic letters, 2014-02, Vol.16 (4), p.1060-1063 [Periódico revisado por pares]

United States: American Chemical Society

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