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Refinado por: Nome da Publicação: The Journal Of Organic Chemistry remover tipo de recurso: Artigos remover
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1
The Goldilocks Principle in Phase Labeling. Minimalist and Orthogonal Phase Tagging for Chromatography-Free Mitsunobu Reaction
The Goldilocks Principle in Phase Labeling. Minimalist and Orthogonal Phase Tagging for Chromatography-Free Mitsunobu Reaction
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The Goldilocks Principle in Phase Labeling. Minimalist and Orthogonal Phase Tagging for Chromatography-Free Mitsunobu Reaction

Szigeti, Mariann ; Dobi, Zoltán ; Soós, Tibor

Journal of organic chemistry, 2018-03, Vol.83 (5), p.2869-2874 [Periódico revisado por pares]

United States: American Chemical Society

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2
Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones
Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones
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Organocatalytic Enantioselective Sulfa-Michael Additions to α,β-Unsaturated Diazoketones

Patrícia Betoni Momo Mizobuchi,Eduardo F; Radell Echemendía; Isabel Baddeley; Matthew N Grayson; Antonio Carlos Bender Burtoloso

The Journal of Organic Chemistry Washington: American Chemical Society v. 87, p. 3482−3490, 2022

Washington 2022

Localização: IQSC - Inst. Química de São Carlos    (P19829 )(Acessar)

3
Scalable, Chromatography-Free Synthesis of Alkyl-Tethered Pyrene-Based Materials. Application to First-Generation “Archipelago Model” Asphaltene Compounds
Scalable, Chromatography-Free Synthesis of Alkyl-Tethered Pyrene-Based Materials. Application to First-Generation “Archipelago Model” Asphaltene Compounds
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Scalable, Chromatography-Free Synthesis of Alkyl-Tethered Pyrene-Based Materials. Application to First-Generation “Archipelago Model” Asphaltene Compounds

Diner, Colin ; Scott, David E ; Tykwinski, Rik R ; Gray, Murray R ; Stryker, Jeffrey M

Journal of organic chemistry, 2015-02, Vol.80 (3), p.1719-1726 [Periódico revisado por pares]

United States: American Chemical Society

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4
Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides
Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides
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Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides

Leandro Alves Bozzini Thiago dos Santos; Valter Eduardo Murie; Murilo B. M Mello; Ricardo Vessecchi; Giuliano Cesar Clososki

The Journal of Organic Chemistry Washington v. 86, n. 1, p. 1204-1215, 2021

Washington 2021

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 3088725 Acervo Digital )(Acessar)

5
Determination of the Absolute Configuration of a Chiral Oxadiazol-3-one Calcium Channel Blocker, Resolved Using Chiral Chromatography, via Concerted Density Functional Theory Calculations of Its Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotation
Determination of the Absolute Configuration of a Chiral Oxadiazol-3-one Calcium Channel Blocker, Resolved Using Chiral Chromatography, via Concerted Density Functional Theory Calculations of Its Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotation
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Determination of the Absolute Configuration of a Chiral Oxadiazol-3-one Calcium Channel Blocker, Resolved Using Chiral Chromatography, via Concerted Density Functional Theory Calculations of Its Vibrational Circular Dichroism, Electronic Circular Dichroism, and Optical Rotation

Stephens, P. J ; Devlin, F. J ; Gasparrini, F ; Ciogli, A ; Spinelli, D ; Cosimelli, B

Journal of organic chemistry, 2007-06, Vol.72 (13), p.4707-4715 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
Screening for Galectin-3 Inhibitors from Synthetic Lacto-N-biose Libraries Using Microscale Affinity Chromatography Coupled to Mass Spectrometry
Screening for Galectin-3 Inhibitors from Synthetic Lacto-N-biose Libraries Using Microscale Affinity Chromatography Coupled to Mass Spectrometry
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Screening for Galectin-3 Inhibitors from Synthetic Lacto-N-biose Libraries Using Microscale Affinity Chromatography Coupled to Mass Spectrometry

Fort, Sébastien ; Kim, Hyo-Sun ; Hindsgaul, Ole

Journal of organic chemistry, 2006-09, Vol.71 (19), p.7146-7154 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Gold(I)-Catalyzed Cascade Cyclization of Alkynyl Indoles for the Stereoselective Construction of the Quaternary Carbon Center of Akuammiline Alkaloids
Gold(I)-Catalyzed Cascade Cyclization of Alkynyl Indoles for the Stereoselective Construction of the Quaternary Carbon Center of Akuammiline Alkaloids
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Gold(I)-Catalyzed Cascade Cyclization of Alkynyl Indoles for the Stereoselective Construction of the Quaternary Carbon Center of Akuammiline Alkaloids

Hashimoto, Naoki ; Taguchi, Junichi ; Arichi, Norihito ; Inuki, Shinsuke ; Ohno, Hiroaki

Journal of organic chemistry, 2023-12, Vol.88 (24), p.17306-17321 [Periódico revisado por pares]

United States: American Chemical Society

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8
Scope of the Two-Step, One-Pot Palladium-Catalyzed Borylation/Suzuki Cross-Coupling Reaction Utilizing Bis-Boronic Acid
Scope of the Two-Step, One-Pot Palladium-Catalyzed Borylation/Suzuki Cross-Coupling Reaction Utilizing Bis-Boronic Acid
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Scope of the Two-Step, One-Pot Palladium-Catalyzed Borylation/Suzuki Cross-Coupling Reaction Utilizing Bis-Boronic Acid

Molander, Gary A ; Trice, Sarah L. J ; Kennedy, Steven M

Journal of organic chemistry, 2012-10, Vol.77 (19), p.8678-8688 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
Organic chemistry of C60 (buckminsterfullerene): chromatography and osmylation
Organic chemistry of C60 (buckminsterfullerene): chromatography and osmylation
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Organic chemistry of C60 (buckminsterfullerene): chromatography and osmylation

Hawkins, Joel M ; Lewis, Timothy A ; Loren, Stefan D ; Meyer, Axel ; Heath, James R ; Shibato, Yoko ; Saykally, Richard J

Journal of organic chemistry, 1990-12, Vol.55 (26), p.6250-6252 [Periódico revisado por pares]

Legacy CDMS: American Chemical Society

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10
Barriers to Stereoinversion of N-Aryl-1,3,2-benzodithiazole 1-Oxides Studied by Dynamic Enantioselective Liquid Chromatography
Barriers to Stereoinversion of N-Aryl-1,3,2-benzodithiazole 1-Oxides Studied by Dynamic Enantioselective Liquid Chromatography
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Barriers to Stereoinversion of N-Aryl-1,3,2-benzodithiazole 1-Oxides Studied by Dynamic Enantioselective Liquid Chromatography

Oxelbark, Joakim ; Allenmark, Stig

Journal of organic chemistry, 1999-03, Vol.64 (5), p.1483-1486 [Periódico revisado por pares]

United States: American Chemical Society

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Deste Autor:

  1. Burtoloso, A
  2. Santos, T
  3. Momo, P
  4. Grayson, M
  5. Echemendía, R

Neste Assunto:

  1. Chemistry
  2. Physical Sciences
  3. Chemistry, Organic
  4. Science & Technology
  5. Organic Chemistry

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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