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Synthesis 2003(5): 0755-0764
DOI: 10.1055/s-2003-38058
DOI: 10.1055/s-2003-38058
SPECIALTOPIC
© Georg Thieme Verlag Stuttgart ˙ New York
Indium-Mediated Allylation Reaction in Aqueous Media: Synthetic Studies Towards the Total Synthesis of Dysiherbaine [1]
Further Information
Received
15 February 2003
Publication Date:
21 March 2003 (online)
Publication History
Publication Date:
21 March 2003 (online)
Abstract
A stereospecific route to the key intermediate 4 for the total synthesis of dysiherbaine has been successfully developed based on the indium-mediated allylation reaction in aqueous media. Further manipulation to the advanced intermediate 28 has resulted in the discovery of a series of highly stereoselective processes.
Key words
indium - allylations - natural products - stereoselectivity - amino acids
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References
HPLC grade solvent used without distillation.