An Alkyne Strategy for the Asymmetric Synthesis of Natural Products: Application to (+)‐Spirolaxine Methyl Ether
Authors:
- 28 September 2007
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 46 (40) , 7664-7666
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Absolute Configuration of the Fungal Metabolite SpirolaxineEuropean Journal of Organic Chemistry, 2005
- Palladium‐Catalyzed DYKAT of Vinyl Epoxides: Enantioselective Total Synthesis and Assignment of the Configuration of (+)‐Broussonetine GAngewandte Chemie, 2003
- Alkoxide-Catalyzed Addition of Terminal Alkynes to KetonesThe Journal of Organic Chemistry, 1996
- Helicobacter pylori: Its Role in DiseaseClinical Infectious Diseases, 1992
- Catalytic asymmetric synthesis of optically active alkynyl alcohols by enantioselective alkynylation of aldehydes and by enantioselective alkylation of alkynyl aldehydesJournal of the Chemical Society, Perkin Transactions 1, 1990
- Amino Alcohol Mediated Enantioselective Addition of 2-Phenylethynylzinc Bromide to AldehydesSynlett, 1990
- Methanolysis of Dimethyl (1-Diazo-2-oxopropyl) Phosphonate: Generation of Dimethyl (Diazomethyl) Phosphonate and Reaction with Carbonyl CompoundsSynthetic Communications, 1989
- Equilibrium acidities in dimethyl sulfoxide solutionAccounts of Chemical Research, 1988
- Transition-metal-catalyzed acetylene cyclizations in organic synthesisAccounts of Chemical Research, 1977
- Ein neuer Katalysator für selektive HydrierungenHelvetica Chimica Acta, 1952