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Generation of acyclic chiral building blocks containing a quaternary stereocenter. Formal synthesis of alkaloids of the leuconolam-leuconoxine-mersicarpine group
Generation of acyclic chiral building blocks containing a quaternary stereocenter. Formal synthesis of alkaloids of the leuconolam-leuconoxine-mersicarpine group
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Generation of acyclic chiral building blocks containing a quaternary stereocenter. Formal synthesis of alkaloids of the leuconolam-leuconoxine-mersicarpine group

Ordeix, Sergi ; Alcaraz, Marta ; Llor, Núria ; Calbó, Arnau ; Bosch, Joan ; Amat, Mercedes

Tetrahedron, 2020-12, Vol.76 (51), p.131017, Article 131017 [Periódico revisado por pares]

Elsevier Ltd

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2
Study of the correlation between blood cholinesterases activity, urinary dialkyl phosphates, and the frequency of micronucleated polychromatic erythrocytes in rats exposed to disulfoton
Study of the correlation between blood cholinesterases activity, urinary dialkyl phosphates, and the frequency of micronucleated polychromatic erythrocytes in rats exposed to disulfoton
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Study of the correlation between blood cholinesterases activity, urinary dialkyl phosphates, and the frequency of micronucleated polychromatic erythrocytes in rats exposed to disulfoton

Santos, Mariane Gonçalves; Vitor, Ricardo Vilela; Nakamura, Maurício Gustavo; Morelini, Luana De Souza; Ferreira, Rafaela Scalco; Paiva, Alexandre Giusti; Azevedo, Luciana; Marques, Vanessa Bergamin Boralli; Martins, Isarita; Figueiredo, Eduardo Costa

Brazilian Journal of Pharmaceutical Sciences; Vol. 49 No. 1 (2013); 149-154

Universidade de São Paulo. Faculdade de Ciências Farmacêuticas 2013-03-01

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3
Selective Fluoromethyl Couplings of Alkynes via Nickel Catalysis
Selective Fluoromethyl Couplings of Alkynes via Nickel Catalysis
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Selective Fluoromethyl Couplings of Alkynes via Nickel Catalysis

Li, Huan ; Wang, Fang ; Zhu, Shengqing ; Chu, Lingling

Angewandte Chemie International Edition, 2022-02, Vol.61 (9), p.e202116725-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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4
Nickel‐Catalyzed Regioselective Intermolecular Dialkylation of Alkenylarenes: Generation of Two Vicinal C(sp3)−C(sp3) Bonds Across Alkenes
Nickel‐Catalyzed Regioselective Intermolecular Dialkylation of Alkenylarenes: Generation of Two Vicinal C(sp3)−C(sp3) Bonds Across Alkenes
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Nickel‐Catalyzed Regioselective Intermolecular Dialkylation of Alkenylarenes: Generation of Two Vicinal C(sp3)−C(sp3) Bonds Across Alkenes

Lux, Daniel M. ; Aryal, Vivek ; Niroula, Doleshwar ; Giri, Ramesh

Angewandte Chemie International Edition, 2023-08, Vol.62 (32), p.e202305522-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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Chiral 1,2,3‐Triazolium Salt Catalyzed Asymmetric Mono‐ and Dialkylation of 2,5‐Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers
Chiral 1,2,3‐Triazolium Salt Catalyzed Asymmetric Mono‐ and Dialkylation of 2,5‐Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers
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Chiral 1,2,3‐Triazolium Salt Catalyzed Asymmetric Mono‐ and Dialkylation of 2,5‐Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers

Yang, Ju‐Song ; Lu, Ka ; Li, Chen‐Xiao ; Zhao, Zu‐Hang ; Zhang, Xiao‐Ming ; Zhang, Fu‐Min ; Tu, Yong‐Qiang

Angewandte Chemie (International ed.), 2022-02, Vol.61 (9), p.e202114129-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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6
Asymmetric Carbene Transformations for the Construction of All‐Carbon Quaternary Centers
Asymmetric Carbene Transformations for the Construction of All‐Carbon Quaternary Centers
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Asymmetric Carbene Transformations for the Construction of All‐Carbon Quaternary Centers

Yao, Minghan ; Dong, Shanliang ; Xu, Xinfang

Chemistry : a European journal, 2024-05, Vol.30 (26), p.e202304299-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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7
Regio‐ and Enantioselective α,γ‐Dialkylation of α,β‐Unsaturated Aldehydes Through Cascade Organocatalysis
Regio‐ and Enantioselective α,γ‐Dialkylation of α,β‐Unsaturated Aldehydes Through Cascade Organocatalysis
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Regio‐ and Enantioselective α,γ‐Dialkylation of α,β‐Unsaturated Aldehydes Through Cascade Organocatalysis

Kutwal, Mahesh S. ; Padmaja, Venkata M. D. ; Appayee, Chandrakumar

European journal of organic chemistry, 2020-05, Vol.2020 (18), p.2720-2724 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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8
Construction of Chiral Quaternary Carbon Centers via Asymmetric Metal Carbene gem‐Dialkylation
Construction of Chiral Quaternary Carbon Centers via Asymmetric Metal Carbene gem‐Dialkylation
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Construction of Chiral Quaternary Carbon Centers via Asymmetric Metal Carbene gem‐Dialkylation

Dong, Shanliang ; Hong, Kemiao ; Zhang, Zhijing ; Huang, Jingjing ; Xie, Xiongda ; Yuan, Haoxuan ; Hu, Wenhao ; Xu, Xinfang

Angewandte Chemie International Edition, 2023-06, Vol.62 (26), p.e202302371-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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9
Practical Methods for the Synthesis of Symmetrically α,α-Disubstituted α-Amino Acids
Practical Methods for the Synthesis of Symmetrically α,α-Disubstituted α-Amino Acids
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Practical Methods for the Synthesis of Symmetrically α,α-Disubstituted α-Amino Acids

Soloshonok, Vadim A. ; Sorochinsky, Alexander E.

Synthesis (Stuttgart), 2010-07, Vol.2010 (14), p.2319-2344 [Periódico revisado por pares]

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10
Hydrazone complexes of ruthenium(II): Synthesis, crystal structures and catalytic applications in N-alkylation reactions
Hydrazone complexes of ruthenium(II): Synthesis, crystal structures and catalytic applications in N-alkylation reactions
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Hydrazone complexes of ruthenium(II): Synthesis, crystal structures and catalytic applications in N-alkylation reactions

Murugan, Kaliyappan ; Vijayapritha, Subbarayan ; Nirmala, Muthukumaran ; Viswanathamurthi, Periasamy ; Natarajan, Karuppannan

Journal of organometallic chemistry, 2020-09, Vol.923, p.121411, Article 121411 [Periódico revisado por pares]

Elsevier B.V

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Deste Autor:

  1. Marques, V
  2. Figueiredo, E
  3. Vitor, R
  4. Paiva, A
  5. Nakamura, M

Neste Assunto:

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

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

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