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The regio- and stereoselective oxyamination of pinenes and camphene
Affiliation:1. Instituto de Quı́mica, GQO, Universidade Federal Fluminense, CEG, Centro, 24210-150 Niterói, RJ, Brazil;2. Laboratório de Quı́mica Bioorgânica (LQB), Núcleo de Pesquisas de Produtos Naturais, Universidade Federal do Rio de Janeiro, CCS, Ilha da Cidade Universitária, 21941-590 Rio de Janeiro, RJ, Brazil;1. Biochemistry, Department of Chemistry, Faculty of Sciences, Hamburg University, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany;2. Organic Chemistry, Department of Chemistry, Faculty of Sciences, Hamburg University, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany;1. Moulder Center for Drug Discovery Research, Temple University School of Pharmacy, 3307 N. Broad Street, Philadelphia, PA, USA;2. Cureveda, LLC, 1450 South Rolling Road, Halethorpe, MD 21227, USA;3. Department of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health, 615 N. Wolfe Street, Baltimore, MD 21205, USA;4. Department of Chemistry, Temple University, Philadelphia, PA 19122, USA
Abstract:The osmium-induced vicinal oxyaminations of pinenes and camphene have been performed with high regio- and stereoselectivities.
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