Search Results - "Childers, Karla G"
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Suzuki-Miyaura Cross-Coupling of 2-Nitroarenediazonium Tetrafluoroborates: Synthesis of Unsymmetrical 2-Nitrobiphenyls and Highly Functionalized Carbazoles
Published in Advanced synthesis & catalysis (07-07-2008)“…The Suzuki–Miyaura cross‐coupling of 2‐nitrodiazonium tetrafluoroborate salts with substituted boronic acids is an effective and efficient means of preparing…”
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Asymmetric Synthesis of a Potent HIV‑1 Integrase Inhibitor
Published in Journal of organic chemistry (04-11-2016)“…The development of a practical asymmetric total synthesis of the potent HIV-1 integrase inhibitor 5 is described. Key transformations include construction of…”
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A Rapid, Large-Scale Synthesis of a Potent Cholecystokinin (CCK) 1R Receptor Agonist
Published in Organic process research & development (21-11-2008)“…The development of a scalable synthesis of a potent cholecystokinin (CCK) 1R receptor agonist is described. The focus on a rapid short-term delivery rather…”
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A Practical, Kilogram-Scale Implementation of the Wolff−Kishner Reduction
Published in Organic process research & development (15-05-2009)“…A safe and practical strategy has been developed for the large-scale preparation of imidazole 7. The key transformation involved the Wolff−Kishner reduction of…”
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A Practical and Scaleable Preparation of 1,4-Anhydroerythritol
Published in Organic process research & development (15-09-2006)“…A practical and efficient kilogram-scale preparation of 1,4-anhydroerythritol from meso-erythritol is described. A novel silica gel and sodium bicarbonate…”
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6
Rearrangement of spiro-benzimidazolines: preparation of N-alkenyl- and N-alkyl-benzimidazol-2-ones
Published in Tetrahedron (12-11-2007)“…A synthetically useful protocol has been developed for the preparation of highly functionalized N-alkenyl-benzimidazol-2-ones. Reaction of commercially…”
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