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1
1,3-dipolar cycloaddition chemistry
1,3-dipolar cycloaddition chemistry
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Livro 		Adicionar ao Meu Espaço

1,3-dipolar cycloaddition chemistry

Albert Padwa 1937-

New York Wiley c1984

Localização: IQSC - Inst. Química de São Carlos    (547.59 P136d v.2 )(Acessar)

2
Hetero Diels-Alder Methodology in Organic Synthesis
Hetero Diels-Alder Methodology in Organic Synthesis
Hetero Diels-Alder Methodology in Organic Synthesis
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Hetero Diels-Alder Methodology in Organic Synthesis

Dale L. Boger Steven M Weinreb

San Diego Elsevier 1987

Acesso online. A biblioteca também possui exemplares impressos.

3
Synthetic applications of 1,3-dipolar cycloaddition chemistry toward heterocycles and natural products
Synthetic applications of 1,3-dipolar cycloaddition chemistry toward heterocycles and natural products
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Synthetic applications of 1,3-dipolar cycloaddition chemistry toward heterocycles and natural products

Albert Padwa 1937-; William H Pearson

Hoboken, NJ Wiley c2003

Localização: CQ - Conjunto das Químicas    (547.2 S9931 )(Acessar)

4
Structure-Based Design of Tricyclic NF-κB Inducing Kinase (NIK) Inhibitors That Have High Selectivity over Phosphoinositide-3-kinase (PI3K)
Structure-Based Design of Tricyclic NF-κB Inducing Kinase (NIK) Inhibitors That Have High Selectivity over Phosphoinositide-3-kinase (PI3K)
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Structure-Based Design of Tricyclic NF-κB Inducing Kinase (NIK) Inhibitors That Have High Selectivity over Phosphoinositide-3-kinase (PI3K)

Castanedo, Georgette M ; Blaquiere, Nicole ; Beresini, Maureen ; Bravo, Brandon ; Brightbill, Hans ; Chen, Jacob ; Cui, Hai-Feng ; Eigenbrot, Charles ; Everett, Christine ; Feng, Jianwen ; Godemann, Robert ; Gogol, Emily ; Hymowitz, Sarah ; Johnson, Adam ; Kayagaki, Nobuhiko ; Kohli, Pawan Bir ; Knüppel, Kathleen ; Kraemer, Joachim ; Krüger, Susan ; Loke, Pui ; McEwan, Paul ; Montalbetti, Christian ; Roberts, David A ; Smith, Myron ; Steinbacher, Stefan ; Sujatha-Bhaskar, Swathi ; Takahashi, Ryan ; Wang, Xiaolu ; Wu, Lawren C ; Zhang, Yamin ; Staben, Steven T

Journal of medicinal chemistry, 2017-01, Vol.60 (2), p.627-640 [Periódico revisado por pares]

United States: American Chemical Society

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5
Chuanxiongdiolides R4 and R5, phthalide dimers with a complex polycyclic skeleton from the aerial parts of Ligusticum chuanxiong and their vasodilator activity
Chuanxiongdiolides R4 and R5, phthalide dimers with a complex polycyclic skeleton from the aerial parts of Ligusticum chuanxiong and their vasodilator activity
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Chuanxiongdiolides R4 and R5, phthalide dimers with a complex polycyclic skeleton from the aerial parts of Ligusticum chuanxiong and their vasodilator activity

Tang, Fei ; Yan, Yong-Ming ; Yan, Hong-Ling ; Wang, Li-Xia ; Hu, Chang-Jiang ; Wang, Hong-Liang ; Ao, Hui ; Peng, Cheng ; Tan, Yu-Zhu

Bioorganic chemistry, 2021-02, Vol.107, p.104523-104523, Article 104523 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Synthesis, characterization and investigation of antibacterial and antifungal activities of novel 1,3-butadiene compounds
Synthesis, characterization and investigation of antibacterial and antifungal activities of novel 1,3-butadiene compounds
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Synthesis, characterization and investigation of antibacterial and antifungal activities of novel 1,3-butadiene compounds

Aydinli, Serdar Goksin ; Ozdamar, Yasemin ; Sayil, Cigdem ; Gulsah Deniz, Nahide ; Stasevych, Maryna ; Zvarych, Viktor ; Komarovska-Porokhnyavets, Olena ; Novikov, Volodymyr

Synthetic communications, 2020-11, Vol.50 (21), p.3234-3244 [Periódico revisado por pares]

Philadelphia: Taylor & Francis

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7
Caged xanthones: Potent inhibitors of global predominant MRSA USA300
Caged xanthones: Potent inhibitors of global predominant MRSA USA300
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Caged xanthones: Potent inhibitors of global predominant MRSA USA300

Chaiyakunvat, Pongkorn ; Anantachoke, Natthinee ; Reutrakul, Vichai ; Jiarpinitnun, Chutima

Bioorganic & medicinal chemistry letters, 2016-07, Vol.26 (13), p.2980-2983 [Periódico revisado por pares]

England: Elsevier Ltd

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8
Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies
Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies
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Structure-Based Design of Highly Potent HIV‑1 Protease Inhibitors Containing New Tricyclic Ring P2-Ligands: Design, Synthesis, Biological, and X‑ray Structural Studies

Ghosh, Arun K ; Kovela, Satish ; Osswald, Heather L ; Amano, Masayuki ; Aoki, Manabu ; Agniswamy, Johnson ; Wang, Yuan-Fang ; Weber, Irene T ; Mitsuya, Hiroaki

J. Med. Chem, 2020-05, Vol.63 (9), p.4867-4879 [Periódico revisado por pares]

United States: American Chemical Society

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9
Design of New Benzo[h]chromene Derivatives: Antitumor Activities and Structure-Activity Relationships of the 2,3-Positions and Fused Rings at the 2,3-Positions
Design of New Benzo[h]chromene Derivatives: Antitumor Activities and Structure-Activity Relationships of the 2,3-Positions and Fused Rings at the 2,3-Positions
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Design of New Benzo[h]chromene Derivatives: Antitumor Activities and Structure-Activity Relationships of the 2,3-Positions and Fused Rings at the 2,3-Positions

Okasha, Rawda M ; Alblewi, Fawzia F ; Afifi, Tarek H ; Naqvi, Arshi ; Fouda, Ahmed M ; Al-Dies, Al-Anood M ; El-Agrody, Ahmed M

Molecules (Basel, Switzerland), 2017-03, Vol.22 (3), p.479 [Periódico revisado por pares]

Switzerland: MDPI AG

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10
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade
Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade
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Total Synthesis of Integrastatin B Enabled by a Benzofuran Oxidative Dearomatization Cascade

More, Atul A ; Ramana, Chepuri V

Organic letters, 2016-03, Vol.18 (6), p.1458-1461 [Periódico revisado por pares]

United States: American Chemical Society

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Deste Autor:

  1. Padwa, A
  2. Pearson, W
  3. Boger, D
  4. Weinreb, S

Neste Assunto:

  1. Chemistry
  2. Organic Chemistry
  3. Science & Technology
  4. Heterocyclic Compounds
  5. Exact Sciences And Technology

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

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