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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
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)

2
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)

3
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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4
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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5
Tolyporphins L–R: Unusual Tetrapyrroles from a Brasilonema sp. of Cyanobacterium
Tolyporphins L–R: Unusual Tetrapyrroles from a Brasilonema sp. of Cyanobacterium
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Tolyporphins L–R: Unusual Tetrapyrroles from a Brasilonema sp. of Cyanobacterium

Gurr, Joshua R ; Dai, Jingqiu ; Philbin, Casey S ; Sartain, Hope T ; O’Donnell, Timothy J ; Yoshida, Wesley Y ; Rheingold, Arnold L ; Williams, Philip G

Journal of organic chemistry, 2020-01, Vol.85 (2), p.318-326 [Periódico revisado por pares]

United States: American Chemical Society

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6
Fmoc-Based Synthesis of Disulfide-Rich Cyclic Peptides
Fmoc-Based Synthesis of Disulfide-Rich Cyclic Peptides
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Fmoc-Based Synthesis of Disulfide-Rich Cyclic Peptides

Cheneval, Olivier ; Schroeder, Christina I ; Durek, Thomas ; Walsh, Phillip ; Huang, Yen-Hua ; Liras, Spiros ; Price, David A ; Craik, David J

Journal of organic chemistry, 2014-06, Vol.79 (12), p.5538-5544 [Periódico revisado por pares]

United States: American Chemical Society

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7
HPLC-Assisted Automated Oligosaccharide Synthesis: Implementation of the Autosampler as a Mode of the Reagent Delivery
HPLC-Assisted Automated Oligosaccharide Synthesis: Implementation of the Autosampler as a Mode of the Reagent Delivery
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HPLC-Assisted Automated Oligosaccharide Synthesis: Implementation of the Autosampler as a Mode of the Reagent Delivery

Pistorio, Salvatore G ; Nigudkar, Swati S ; Stine, Keith J ; Demchenko, Alexei V

Journal of organic chemistry, 2016-10, Vol.81 (19), p.8796-8805 [Periódico revisado por pares]

United States: American Chemical Society

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8
A Guide to Sonogashira Cross-Coupling Reactions: The Influence of Substituents in Aryl Bromides, Acetylenes, and Phosphines
A Guide to Sonogashira Cross-Coupling Reactions: The Influence of Substituents in Aryl Bromides, Acetylenes, and Phosphines
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A Guide to Sonogashira Cross-Coupling Reactions: The Influence of Substituents in Aryl Bromides, Acetylenes, and Phosphines

Schilz, Marc ; Plenio, Herbert

Journal of organic chemistry, 2012-03, Vol.77 (6), p.2798-2807 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
C3 Epimerization of Glucose, via Regioselective Oxidation and Reduction
C3 Epimerization of Glucose, via Regioselective Oxidation and Reduction
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C3 Epimerization of Glucose, via Regioselective Oxidation and Reduction

Jumde, Varsha R ; Eisink, Niek N. H. M ; Witte, Martin D ; Minnaard, Adriaan J

Journal of organic chemistry, 2016-11, Vol.81 (22), p.11439-11443 [Periódico revisado por pares]

United States: American Chemical Society

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10
Synthesis, Resolution, Structure, and Racemization of Inherently Chiral 1,3-Alternate Azacalix[4]pyrimidines: Quantification of Conformation Mobility
Synthesis, Resolution, Structure, and Racemization of Inherently Chiral 1,3-Alternate Azacalix[4]pyrimidines: Quantification of Conformation Mobility
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Synthesis, Resolution, Structure, and Racemization of Inherently Chiral 1,3-Alternate Azacalix[4]pyrimidines: Quantification of Conformation Mobility

Li, Jiang-Tao ; Wang, Li-Xia ; Wang, De-Xian ; Zhao, Liang ; Wang, Mei-Xiang

Journal of organic chemistry, 2014-03, Vol.79 (5), p.2178-2188 [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. Organic Chemistry
  2. Chemistry
  3. Physical Sciences
  4. Chemistry, Organic
  5. Science & Technology

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

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