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Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones
Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones
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Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones

Thiago dos Santos Caroline Grundke; Tobias Lucas; Luca Großmann; Giuliano Cesar Clososki; Till Opatz

European Journal of Organic Chemistry Weinheim v. 2020, n. 41, p. 6429-6432, 2020

Weinheim 2020

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 3096911 Acervo Digital )(Acessar)

2
Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones
Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones
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Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones

Thiago dos Santos Caroline Grundke; Tobias Lucas; Luca Großmann; Giuliano Cesar Clososki; Till Opatz

European Journal of Organic Chemistry Weinheim v. 2020, n. 41, p. 6429-6432, 2020

Weinheim 2020

Localização: FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (pcd 3143006 Acervo Digital )(Acessar)

3
Iodine‐Mediated Domino C(sp2)–H Sulfonylation/Annulation of Enaminones and Sulfonyl Hydrazines for the Synthesis of 3‐Sulfonyl Chromones
Iodine‐Mediated Domino C(sp2)–H Sulfonylation/Annulation of Enaminones and Sulfonyl Hydrazines for the Synthesis of 3‐Sulfonyl Chromones
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Iodine‐Mediated Domino C(sp2)–H Sulfonylation/Annulation of Enaminones and Sulfonyl Hydrazines for the Synthesis of 3‐Sulfonyl Chromones

Wan, Jie‐Ping ; Zhong, Shanshan ; Guo, Yanhui ; Wei, Li

European journal of organic chemistry, 2017-08, Vol.2017 (30), p.4401-4404 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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4
Stereoselective Synthesis of 1,2‐Annulated Sugars Having Substituted Tetrahydropyran/(‐furan) Scaffolds Using the Prins‐Reaction
Stereoselective Synthesis of 1,2‐Annulated Sugars Having Substituted Tetrahydropyran/(‐furan) Scaffolds Using the Prins‐Reaction
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Stereoselective Synthesis of 1,2‐Annulated Sugars Having Substituted Tetrahydropyran/(‐furan) Scaffolds Using the Prins‐Reaction

Chennaiah, Ande ; Dubbu, Sateesh ; Parasuraman, Kadigachalam ; Vankar, Yashwant D.

European journal of organic chemistry, 2018-12, Vol.2018 (47), p.6706-6713 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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5
Pseudo‐Solid‐State Suzuki–Miyaura Reaction and the Role of Water Formed by Dehydration of Arylboronic Acids
Pseudo‐Solid‐State Suzuki–Miyaura Reaction and the Role of Water Formed by Dehydration of Arylboronic Acids
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Pseudo‐Solid‐State Suzuki–Miyaura Reaction and the Role of Water Formed by Dehydration of Arylboronic Acids

Pentsak, Evgeniy O. ; Ananikov, Valentine P.

European journal of organic chemistry, 2019-07, Vol.2019 (26), p.4239-4247 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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6
Recent Advances in Intramolecular Metal‐Free Oxidative C–H Bond Aminations Using Hypervalent Iodine(III) Reagents
Recent Advances in Intramolecular Metal‐Free Oxidative C–H Bond Aminations Using Hypervalent Iodine(III) Reagents
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Recent Advances in Intramolecular Metal‐Free Oxidative C–H Bond Aminations Using Hypervalent Iodine(III) Reagents

Reddy Kandimalla, Satheeshkumar ; Prathima Parvathaneni, Sai ; Sabitha, Gowravaram ; Subba Reddy, B. V.

European journal of organic chemistry, 2019-02, Vol.2019 (8), p.1687-1714 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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7
Ugi Reaction Followed by Intramolecular Diels–Alder Reaction and Elimination of HCl: One‐Pot Approach to Arene‐Fused Isoindolinones
Ugi Reaction Followed by Intramolecular Diels–Alder Reaction and Elimination of HCl: One‐Pot Approach to Arene‐Fused Isoindolinones
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Ugi Reaction Followed by Intramolecular Diels–Alder Reaction and Elimination of HCl: One‐Pot Approach to Arene‐Fused Isoindolinones

Huang, Jianjun ; Du, Xiaochen ; Van Hecke, Kristof ; Van der Eycken, Erik V. ; Pereshivko, Olga P. ; Peshkov, Vsevolod A.

European journal of organic chemistry, 2017-08, Vol.2017 (30), p.4379-4388 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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8
DEAD‐Promoted Oxidative Ugi‐Type Reaction Including an Unprecedented Ugi Amidation Assisted by Dicarboxylic Acids
DEAD‐Promoted Oxidative Ugi‐Type Reaction Including an Unprecedented Ugi Amidation Assisted by Dicarboxylic Acids
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DEAD‐Promoted Oxidative Ugi‐Type Reaction Including an Unprecedented Ugi Amidation Assisted by Dicarboxylic Acids

Wang, Jiankun ; Sun, Yilin ; Wang, Guangji ; Zhen, Le

European journal of organic chemistry, 2017-11, Vol.2017 (42), p.6338-6348 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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9
Chroman‐4‐one‐Based Amino Bidentate Ligand: An Efficient Ligand for Suzuki‐Miyaura and Mizoroki‐Heck Coupling Reactions in Aqueous Medium
Chroman‐4‐one‐Based Amino Bidentate Ligand: An Efficient Ligand for Suzuki‐Miyaura and Mizoroki‐Heck Coupling Reactions in Aqueous Medium
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Chroman‐4‐one‐Based Amino Bidentate Ligand: An Efficient Ligand for Suzuki‐Miyaura and Mizoroki‐Heck Coupling Reactions in Aqueous Medium

Khan, Danish ; Parveen, Iram

European journal of organic chemistry, 2021-09, Vol.2021 (35), p.4946-4957 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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10
Catalytic Enantioselective Aza-Henry Reactions
Catalytic Enantioselective Aza-Henry Reactions
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Catalytic Enantioselective Aza-Henry Reactions

Marqués-López, Eugenia ; Merino, Pedro ; Tejero, Tomás ; Herrera, Raquel P.

European Journal of Organic Chemistry, 2009-05, Vol.2009 (15), p.2401-2420 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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Deste Autor:

  1. Lucas, T
  2. Opatz, T
  3. Clososki, G
  4. Großmann, L
  5. Grundke, C

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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