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Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes
Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes
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Iron Catalysts for Selective Anti-Markovnikov Alkene Hydrosilylation Using Tertiary Silanes

Tondreau, Aaron M. ; Atienza, Crisita Carmen Hojilla ; Weller, Keith J. ; Nye, Susan A. ; Lewis, Kenrick M. ; Delis, Johannes G. P. ; Chirik, Paul J.

Science (American Association for the Advancement of Science), 2012-02, Vol.335 (6068), p.567-570 [Periódico revisado por pares]

Washington, DC: American Association for the Advancement of Science

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From σ- to π-Electrophilic Lewis Acids. Application to Selective Organic Transformations
From σ- to π-Electrophilic Lewis Acids. Application to Selective Organic Transformations
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From σ- to π-Electrophilic Lewis Acids. Application to Selective Organic Transformations

Yamamoto, Yoshinori

Journal of organic chemistry, 2007-10, Vol.72 (21), p.7817-7831 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
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Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos

Martinelli, Joseph R ; Watson, Donald A ; Freckmann, Dominique M. M ; Barder, Timothy E ; Buchwald, Stephen L

Journal of organic chemistry, 2008-09, Vol.73 (18), p.7102-7107 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
N-Alkylation of poor nucleophilic amines and derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper(II) acetate: scope and mechanistic considerations
N-Alkylation of poor nucleophilic amines and derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper(II) acetate: scope and mechanistic considerations
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N-Alkylation of poor nucleophilic amines and derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper(II) acetate: scope and mechanistic considerations

Martínez-Asencio, Ana ; Ramón, Diego J. ; Yus, Miguel

Tetrahedron, 2011-04, Vol.67 (17), p.3140-3149 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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5
Isolable Gold(I) Complexes Having One Low-Coordinating Ligand as Catalysts for the Selective Hydration of Substituted Alkynes at Room Temperature without Acidic Promoters
Isolable Gold(I) Complexes Having One Low-Coordinating Ligand as Catalysts for the Selective Hydration of Substituted Alkynes at Room Temperature without Acidic Promoters
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Isolable Gold(I) Complexes Having One Low-Coordinating Ligand as Catalysts for the Selective Hydration of Substituted Alkynes at Room Temperature without Acidic Promoters

Leyva, Antonio ; Corma, Avelino

Journal of organic chemistry, 2009-03, Vol.74 (5), p.2067-2074 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Perspective on Dirhodium Carboxamidates as Catalysts
Perspective on Dirhodium Carboxamidates as Catalysts
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Perspective on Dirhodium Carboxamidates as Catalysts

Doyle, Michael P

Journal of organic chemistry, 2006-12, Vol.71 (25), p.9253-9260 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
DFT and Experimental Exploration of the Mechanism of InCl3‑Catalyzed Type II Cycloisomerization of 1,6-Enynes: Identifying InCl2 + as the Catalytic Species and Answering Why Nonconjugated Dienes Are Generated
DFT and Experimental Exploration of the Mechanism of InCl3‑Catalyzed Type II Cycloisomerization of 1,6-Enynes: Identifying InCl2 + as the Catalytic Species and Answering Why Nonconjugated Dienes Are Generated
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DFT and Experimental Exploration of the Mechanism of InCl3‑Catalyzed Type II Cycloisomerization of 1,6-Enynes: Identifying InCl2 + as the Catalytic Species and Answering Why Nonconjugated Dienes Are Generated

Zhuo, Lian-Gang ; Zhang, Ji-Ji ; Yu, Zhi-Xiang

Journal of organic chemistry, 2012-10, Vol.77 (19), p.8527-8540 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings
Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings
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Air Stable, Sterically Hindered Ferrocenyl Dialkylphosphines for Palladium-Catalyzed C−C, C−N, and C−O Bond-Forming Cross-Couplings

Kataoka, Noriyasu ; Shelby, Quinetta ; Stambuli, James P ; Hartwig, John F

Journal of organic chemistry, 2002-08, Vol.67 (16), p.5553-5566 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
Asymmetric Reduction of Imines with Trichlorosilane, Catalyzed by Sigamide, an Amino Acid-Derived Formamide: Scope and Limitations
Asymmetric Reduction of Imines with Trichlorosilane, Catalyzed by Sigamide, an Amino Acid-Derived Formamide: Scope and Limitations
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Asymmetric Reduction of Imines with Trichlorosilane, Catalyzed by Sigamide, an Amino Acid-Derived Formamide: Scope and Limitations

Malkov, Andrei V ; Vranková, Kvetoslava ; Stončius, Sigitas ; Kočovský, Pavel

Journal of organic chemistry, 2009-08, Vol.74 (16), p.5839-5849 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
Nickel-Catalyzed Amination of Aryl Tosylates
Nickel-Catalyzed Amination of Aryl Tosylates
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Nickel-Catalyzed Amination of Aryl Tosylates

Gao, Cai-Yan ; Yang, Lian-Ming

Journal of organic chemistry, 2008-02, Vol.73 (4), p.1624-1627 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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