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Refinado por: Nome da Publicação: Organic Letters remover
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1
1-Naphthylpropargyl Ether Group:  A Readily Cleaved and Sterically Minimal Protecting System for Stereoselective Glycosylation
1-Naphthylpropargyl Ether Group:  A Readily Cleaved and Sterically Minimal Protecting System for Stereoselective Glycosylation
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1-Naphthylpropargyl Ether Group:  A Readily Cleaved and Sterically Minimal Protecting System for Stereoselective Glycosylation

Crich, David ; Wu, Baolin

Organic letters, 2006-10, Vol.8 (21), p.4879-4882 [Periódico revisado por pares]

United States: American Chemical Society

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2
1-tert-Butoxy-2-tert-butoxycarbonyl- 1,2-dihydroisoquinoline:  A Novel and Chemoselective tert-Butoxycarbonylation Reagent
1-tert-Butoxy-2-tert-butoxycarbonyl- 1,2-dihydroisoquinoline:  A Novel and Chemoselective tert-Butoxycarbonylation Reagent
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1-tert-Butoxy-2-tert-butoxycarbonyl- 1,2-dihydroisoquinoline:  A Novel and Chemoselective tert-Butoxycarbonylation Reagent

Ouchi, Hidekazu ; Saito, Yukako ; Yamamoto, Yutaka ; Takahata, Hiroki

Organic letters, 2002-02, Vol.4 (4), p.585-587 [Periódico revisado por pares]

United States: American Chemical Society

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3
1,1-Carboboration of 1-Alkynes: A Conceptual Alternative to the Hydroboration Reaction
1,1-Carboboration of 1-Alkynes: A Conceptual Alternative to the Hydroboration Reaction
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1,1-Carboboration of 1-Alkynes: A Conceptual Alternative to the Hydroboration Reaction

Chen, Chao ; Voss, Tanja ; Fröhlich, Roland ; Kehr, Gerald ; Erker, Gerhard

Organic letters, 2011-01, Vol.13 (1), p.62-65 [Periódico revisado por pares]

United States: American Chemical Society

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4
1,2-Benzothiazines from Sulfoximines and Allyl Methyl Carbonate by Rhodium-Catalyzed Cross-Coupling and Oxidative Cyclization
1,2-Benzothiazines from Sulfoximines and Allyl Methyl Carbonate by Rhodium-Catalyzed Cross-Coupling and Oxidative Cyclization
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1,2-Benzothiazines from Sulfoximines and Allyl Methyl Carbonate by Rhodium-Catalyzed Cross-Coupling and Oxidative Cyclization

Wen, Jian ; Tiwari, Deo Prakash ; Bolm, Carsten

Organic letters, 2017-04, Vol.19 (7), p.1706-1709 [Periódico revisado por pares]

United States: American Chemical Society

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5
1,2-Bis(diphenylphosphino)carborane As a Dual Mode Ligand for Both the Sonogashira Coupling and Hydride-Transfer Steps in Palladium-Catalyzed One-Pot Synthesis of Allenes from Aryl Iodides
1,2-Bis(diphenylphosphino)carborane As a Dual Mode Ligand for Both the Sonogashira Coupling and Hydride-Transfer Steps in Palladium-Catalyzed One-Pot Synthesis of Allenes from Aryl Iodides
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1,2-Bis(diphenylphosphino)carborane As a Dual Mode Ligand for Both the Sonogashira Coupling and Hydride-Transfer Steps in Palladium-Catalyzed One-Pot Synthesis of Allenes from Aryl Iodides

Nakamura, Hiroyuki ; Kamakura, Takaya ; Onagi, Shinya

Organic letters, 2006-05, Vol.8 (10), p.2095-2098 [Periódico revisado por pares]

United States: American Chemical Society

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6
1,2-H Shift in Copper−Chlorocarbenoid Intermediate during CuCl/bpy-Promoted Stereoselective Dechlorination of 2,2,2-Trichloroethyl Alkyl Ethers to (Z)-1-Alkoxy-2-chloroethenes
1,2-H Shift in Copper−Chlorocarbenoid Intermediate during CuCl/bpy-Promoted Stereoselective Dechlorination of 2,2,2-Trichloroethyl Alkyl Ethers to (Z)-1-Alkoxy-2-chloroethenes
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1,2-H Shift in Copper−Chlorocarbenoid Intermediate during CuCl/bpy-Promoted Stereoselective Dechlorination of 2,2,2-Trichloroethyl Alkyl Ethers to (Z)-1-Alkoxy-2-chloroethenes

Ram, Ram N ; Manoj, T. P

Organic letters, 2008-06, Vol.10 (11), p.2243-2246 [Periódico revisado por pares]

United States: American Chemical Society

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7
1,2,3-Triazole Bound Au(I) (TA-Au) as Chemoselective Catalysts in Promoting Asymmetric Synthesis of Substituted Allenes
1,2,3-Triazole Bound Au(I) (TA-Au) as Chemoselective Catalysts in Promoting Asymmetric Synthesis of Substituted Allenes
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1,2,3-Triazole Bound Au(I) (TA-Au) as Chemoselective Catalysts in Promoting Asymmetric Synthesis of Substituted Allenes

Wang, Dawei ; Gautam, Lekh Nath S ; Bollinger, Cynthia ; Harris, Aleksandra ; Li, Minyong ; Shi, Xiaodong

Organic letters, 2011-05, Vol.13 (10), p.2618-2621 [Periódico revisado por pares]

United States: American Chemical Society

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8
1,3,5-Trisubstituted and 5-Acyl-1,3-Disubstituted Hydantoin Derivatives via Novel Sequential Three-Component Reaction
1,3,5-Trisubstituted and 5-Acyl-1,3-Disubstituted Hydantoin Derivatives via Novel Sequential Three-Component Reaction
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1,3,5-Trisubstituted and 5-Acyl-1,3-Disubstituted Hydantoin Derivatives via Novel Sequential Three-Component Reaction

Attanasi, Orazio A. ; Crescentini, Lucia De ; Favi, Gianfranco ; Nicolini, Simona ; Perrulli, Francesca Romana ; Santeusanio, Stefania

Organic letters, 2011-02, Vol.13 (3), p.353-355 [Periódico revisado por pares]

United States: American Chemical Society

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9
1,4-Hydrogen Radical Transfer as a New and Versatile Tool for the Synthesis of Enantiomerically Pure 1,2,3-Triols
1,4-Hydrogen Radical Transfer as a New and Versatile Tool for the Synthesis of Enantiomerically Pure 1,2,3-Triols
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1,4-Hydrogen Radical Transfer as a New and Versatile Tool for the Synthesis of Enantiomerically Pure 1,2,3-Triols

Gulea, Mihaela ; López-Romero, Juan Manuel ; Fensterbank, Louis ; Malacria, Max

Organic letters, 2000-08, Vol.2 (17), p.2591-2594 [Periódico revisado por pares]

United States: American Chemical Society

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10
1,4-Naphthoquinones in H‑Bond-Directed Trienamine-Mediated Strategies
1,4-Naphthoquinones in H‑Bond-Directed Trienamine-Mediated Strategies
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1,4-Naphthoquinones in H‑Bond-Directed Trienamine-Mediated Strategies

Albrecht, Łukasz ; Gómez, Clarisa Villegas ; Jacobsen, Christian Borch ; Jørgensen, Karl Anker

Organic letters, 2013-06, Vol.15 (12), p.3010-3013 [Periódico revisado por pares]

United States: American Chemical Society

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