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Total Synthesis of (+)-Fawcettimine.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 40, p. 7671, doi. 10.1002/anie.200702695
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- Article
Enantioselective Reduction of Ketones and Imines Catalyzed by (CN-Box)Re<sup>V</sup>-Oxo Complexes.
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- Chemistry - A European Journal, 2010, v. 16, n. 31, p. 9555, doi. 10.1002/chem.201001164
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- Article
Gold(I)-Catalyzed 5-endo-dig Carbocyclization of Acetylenic Dicarbonyl CompoundsWe gratefully acknowledge the University of California, Berkeley, Merck Research Laboratories, and Amgen Inc. for financial support. J.J.K.-S. thanks Eli Lilly & Co. for a graduate fellowship. The Center for New Directions in Organic Synthesis is supported by Bristol-Myers Squibb as a Sponsoring Member and Novartis Pharma as a Supporting Member.
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- Angewandte Chemie, 2004, v. 116, n. 40, p. 5464, doi. 10.1002/ange.200460844
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- Article
Gold(I)-Catalyzed Cyclizations of Silyl Enol Ethers: Application to the Synthesis of (+)-Lycopladine AWe gratefully acknowledge the University of California, Berkeley, NIHGMS (R01 GM073932-01), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Pfizer, AstraZeneca, and Roche for financial support. J.J.K.-S. thanks Eli Lilly & Co. for a graduate fellowship. We thank Lauren A. Young for the preparation of tributylallenylstannane.
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- Angewandte Chemie, 2006, v. 118, n. 36, p. 6137, doi. 10.1002/ange.200602035
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- Article
Cover Picture: Diphenyl Ether Non-Nucleoside Reverse Transcriptase Inhibitors with Excellent Potency Against Resistant Mutant Viruses and Promising Pharmacokinetic Properties (ChemMedChem 1/2009).
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- ChemMedChem, 2009, v. 4, n. 1, p. 1, doi. 10.1002/cmdc.200990000
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- Article
Diphenyl Ether Non-Nucleoside Reverse Transcriptase Inhibitors with Excellent Potency Against Resistant Mutant Viruses and Promising Pharmacokinetic Properties.
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- ChemMedChem, 2009, v. 4, n. 1, p. 88, doi. 10.1002/cmdc.200800262
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- Article
Gold(I)-Catalyzed Cyclizations of Silyl Enol Ethers: Application to the Synthesis of (+)-Lycopladine AWe gratefully acknowledge the University of California, Berkeley, NIHGMS (R01 GM073932-01), Merck Research Laboratories, Bristol-Myers Squibb, Amgen Inc., DuPont, GlaxoSmithKline, Eli Lilly & Co., Pfizer, AstraZeneca, and Roche for financial support. J.J.K.-S. thanks Eli Lilly & Co. for a graduate fellowship. We thank Lauren A. Young for the preparation of tributylallenylstannane.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 36, p. 5991, doi. 10.1002/anie.200602035
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- Publication type:
- Article
Gold( I)-Catalyzed 5- endo- dig Carbocyclization of Acetylenic Dicarbonyl Compounds.
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 40, p. 5350, doi. 10.1002/anie.200460844
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- Article