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Refinado por: Base de dados/Biblioteca: American Chemical Society (ACS) Open Access remover Nome da Publicação: Journal Of Organic Chemistry remover
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1
2,2,2-Trifluoroacetophenone: An Organocatalyst for an Environmentally Friendly Epoxidation of Alkenes
2,2,2-Trifluoroacetophenone: An Organocatalyst for an Environmentally Friendly Epoxidation of Alkenes
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2,2,2-Trifluoroacetophenone: An Organocatalyst for an Environmentally Friendly Epoxidation of Alkenes

Limnios, Dimitris ; Kokotos, Christoforos G

Journal of organic chemistry, 2014-05, Vol.79 (10), p.4270-4276 [Periódico revisado por pares]

United States: American Chemical Society

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2
(2S,4R)‑4-Hydroxyproline(4-nitrobenzoate): Strong Induction of Stereoelectronic Effects via a Readily Synthesized Proline Derivative. Crystallographic Observation of a Correlation between Torsion Angle and Bond Length in a Hyperconjugative Interaction
(2S,4R)‑4-Hydroxyproline(4-nitrobenzoate): Strong Induction of Stereoelectronic Effects via a Readily Synthesized Proline Derivative. Crystallographic Observation of a Correlation between Torsion Angle and Bond Length in a Hyperconjugative Interaction
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(2S,4R)‑4-Hydroxyproline(4-nitrobenzoate): Strong Induction of Stereoelectronic Effects via a Readily Synthesized Proline Derivative. Crystallographic Observation of a Correlation between Torsion Angle and Bond Length in a Hyperconjugative Interaction

Pandey, Anil K ; Yap, Glenn P. A ; Zondlo, Neal J

Journal of organic chemistry, 2014-05, Vol.79 (9), p.4174-4179 [Periódico revisado por pares]

United States: American Chemical Society

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3
3‑Chloro-1-lithiopropene, a Functional Organolithium Reagent, and Its Reactions with Alkylboronates To Give 3‑Alkylprop-1-en-3-ols
3‑Chloro-1-lithiopropene, a Functional Organolithium Reagent, and Its Reactions with Alkylboronates To Give 3‑Alkylprop-1-en-3-ols
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3‑Chloro-1-lithiopropene, a Functional Organolithium Reagent, and Its Reactions with Alkylboronates To Give 3‑Alkylprop-1-en-3-ols

Smith, Keith ; Elliott, Mark C ; Jones, D. Heulyn

Journal of organic chemistry, 2013-09, Vol.78 (18), p.9526-9531 [Periódico revisado por pares]

United States: American Chemical Society

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4
3‑Fluoroazetidinecarboxylic Acids and trans,trans-3,4-Difluoroproline as Peptide Scaffolds: Inhibition of Pancreatic Cancer Cell Growth by a Fluoroazetidine Iminosugar
3‑Fluoroazetidinecarboxylic Acids and trans,trans-3,4-Difluoroproline as Peptide Scaffolds: Inhibition of Pancreatic Cancer Cell Growth by a Fluoroazetidine Iminosugar
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3‑Fluoroazetidinecarboxylic Acids and trans,trans-3,4-Difluoroproline as Peptide Scaffolds: Inhibition of Pancreatic Cancer Cell Growth by a Fluoroazetidine Iminosugar

Liu, Zilei ; Jenkinson, Sarah F ; Vermaas, Tom ; Adachi, Isao ; Wormald, Mark R ; Hata, Yukako ; Kurashima, Yukiko ; Kaji, Akira ; Yu, Chu-Yi ; Kato, Atsushi ; Fleet, George W. J

Journal of organic chemistry, 2015-05, Vol.80 (9), p.4244-4258 [Periódico revisado por pares]

United States: American Chemical Society

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5
5‑Carboxamido-5-formamido-2-iminohydantoin, in Addition to 8‑oxo-7,8-Dihydroguanine, Is the Major Product of the Iron-Fenton or X‑ray Radiation-Induced Oxidation of Guanine under Aerobic Reducing Conditions in Nucleoside and DNA Contexts
5‑Carboxamido-5-formamido-2-iminohydantoin, in Addition to 8‑oxo-7,8-Dihydroguanine, Is the Major Product of the Iron-Fenton or X‑ray Radiation-Induced Oxidation of Guanine under Aerobic Reducing Conditions in Nucleoside and DNA Contexts
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5‑Carboxamido-5-formamido-2-iminohydantoin, in Addition to 8‑oxo-7,8-Dihydroguanine, Is the Major Product of the Iron-Fenton or X‑ray Radiation-Induced Oxidation of Guanine under Aerobic Reducing Conditions in Nucleoside and DNA Contexts

Alshykhly, Omar R ; Fleming, Aaron M ; Burrows, Cynthia J

Journal of organic chemistry, 2015-07, Vol.80 (14), p.6996-7007 [Periódico revisado por pares]

United States: American Chemical Society

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6
A 6′-Fluoro-Substituent in Bicyclo-DNA Increases Affinity to Complementary RNA Presumably by CF–HC Pseudohydrogen Bonds
A 6′-Fluoro-Substituent in Bicyclo-DNA Increases Affinity to Complementary RNA Presumably by CF–HC Pseudohydrogen Bonds
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A 6′-Fluoro-Substituent in Bicyclo-DNA Increases Affinity to Complementary RNA Presumably by CF–HC Pseudohydrogen Bonds

Dugovic, Branislav ; Leumann, Christian J

Journal of organic chemistry, 2014-02, Vol.79 (3), p.1271-1279 [Periódico revisado por pares]

United States: American Chemical Society

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7
Acceleration Effects of Phosphine Ligands on the Rhodium-Catalyzed Dehydrogenative Silylation and Germylation of Unactivated C(sp3)–H Bonds
Acceleration Effects of Phosphine Ligands on the Rhodium-Catalyzed Dehydrogenative Silylation and Germylation of Unactivated C(sp3)–H Bonds
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Acceleration Effects of Phosphine Ligands on the Rhodium-Catalyzed Dehydrogenative Silylation and Germylation of Unactivated C(sp3)–H Bonds

Murai, Masahito ; Takeshima, Hirotaka ; Morita, Haruka ; Kuninobu, Yoichiro ; Takai, Kazuhiko

Journal of organic chemistry, 2015-06, Vol.80 (11), p.5407-5414 [Periódico revisado por pares]

United States: American Chemical Society

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8
Accessing 2,1-Borazaronaphthols: Self-Arylation of 1‑Alkyl-2-aryl-3-bromo-2,1-borazaronaphthalenes
Accessing 2,1-Borazaronaphthols: Self-Arylation of 1‑Alkyl-2-aryl-3-bromo-2,1-borazaronaphthalenes
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Accessing 2,1-Borazaronaphthols: Self-Arylation of 1‑Alkyl-2-aryl-3-bromo-2,1-borazaronaphthalenes

Molander, Gary A ; Wisniewski, Steven R

Journal of organic chemistry, 2014-09, Vol.79 (17), p.8339-8347 [Periódico revisado por pares]

United States: American Chemical Society

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9
Accessing Molecularly Complex Azaborines: Palladium-Catalyzed Suzuki–Miyaura Cross-Couplings of Brominated 2,1-Borazaronaphthalenes and Potassium Organotrifluoroborates
Accessing Molecularly Complex Azaborines: Palladium-Catalyzed Suzuki–Miyaura Cross-Couplings of Brominated 2,1-Borazaronaphthalenes and Potassium Organotrifluoroborates
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Accessing Molecularly Complex Azaborines: Palladium-Catalyzed Suzuki–Miyaura Cross-Couplings of Brominated 2,1-Borazaronaphthalenes and Potassium Organotrifluoroborates

Molander, Gary A ; Wisniewski, Steven R

Journal of organic chemistry, 2014-07, Vol.79 (14), p.6663-6678 [Periódico revisado por pares]

United States: American Chemical Society

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10
Alcohol Cross-Coupling for the Kinetic Resolution of Diols via Oxidative Esterification
Alcohol Cross-Coupling for the Kinetic Resolution of Diols via Oxidative Esterification
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Alcohol Cross-Coupling for the Kinetic Resolution of Diols via Oxidative Esterification

Hofmann, Christine ; Schümann, Jan M ; Schreiner, Peter R

Journal of organic chemistry, 2015-02, Vol.80 (3), p.1972-1978 [Periódico revisado por pares]

United States: American Chemical Society

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