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Cover Picture: CC Cross-Coupling Reactions of O<sup>6</sup>-Alkyl-2-Haloinosine Derivatives and a One-Pot Cross-Coupling/ O<sup>6</sup>-Deprotection Procedure (Chem. Asian J. 8/2012).
- Published in:
- Chemistry - An Asian Journal, 2012, v. 7, n. 8, p. 1725, doi. 10.1002/asia.201290030
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- Article
CC Cross-Coupling Reactions of O<sup>6</sup>-Alkyl-2-Haloinosine Derivatives and a One-Pot Cross-Coupling/ O<sup>6</sup>-Deprotection Procedure.
- Published in:
- Chemistry - An Asian Journal, 2012, v. 7, n. 8, p. 1853, doi. 10.1002/asia.201200093
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- Article
Pd-Catalyzed versus Uncatalyzed, PhI(OAc)<sub>2</sub>-Mediated Cyclization Reactions of N<sup>6</sup>-([1,1′-Biaryl]-2-yl)Adenine Nucleosides.
- Published in:
- ChemCatChem, 2017, v. 9, n. 21, p. 4017, doi. 10.1002/cctc.201701686
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Front Cover: Pd-Catalyzed versus Uncatalyzed, PhI(OAc)<sub>2</sub>-Mediated Cyclization Reactions of N<sup>6</sup>-([1,1′-Biaryl]-2-yl)Adenine Nucleosides (ChemCatChem 21/2017).
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- ChemCatChem, 2017, v. 9, n. 21, p. 4014, doi. 10.1002/cctc.201701672
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- Article
Pd-Catalyzed versus Uncatalyzed, PhI(OAc)<sub>2</sub>-Mediated Cyclization Reactions of N<sup>6</sup>-([1,1′-Biaryl]-2-yl)Adenine Nucleosides.
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- ChemCatChem, 2017, v. 9, n. 21, p. 4058, doi. 10.1002/cctc.201700918
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- Article
Cu-free Sonogashira Type Cross-Coupling of 6-Halo-2-cyclopropyl-3-(pyridyl-3-ylmethyl) Quinazolin-4(3 H)-ones as Potential Antimicrobial Agents.
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- Journal of Heterocyclic Chemistry, 2017, v. 54, n. 4, p. 2272, doi. 10.1002/jhet.2815
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- Article
The Disappearing Director: The Case of Directed N‐Arylation via a Removable Hydroxyl Group.
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- Advanced Synthesis & Catalysis, 2018, v. 360, n. 13, p. 2503, doi. 10.1002/adsc.201701611
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- Article
Mild and General Access to Diverse 1 H-Benzotriazoles via Diboron-Mediated NOH Deoxygenation and Palladium- Catalyzed CC and CN Bond Formation.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 2/3, p. 451, doi. 10.1002/adsc.201400889
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- Article
Cladribine Analogues via O<sup>6</sup>-(Benzotriazolyl) Derivatives of Guanine Nucleosides.
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- Molecules, 2015, v. 20, n. 10, p. 18437, doi. 10.3390/molecules201018437
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- Article