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Synlett 2010(6): 982-986
DOI: 10.1055/s-0029-1219540
DOI: 10.1055/s-0029-1219540
LETTER
© Georg Thieme Verlag
Stuttgart ˙ New York
Exploratory Studies en Route to 5-Alkyl-Hyacinthacines: Synthesis of 5-epi-(-)-Hyacinthacine A3 and (-)-Hyacinthacine A3
Further Information
Received
22 December 2009
Publication Date:
23 February 2010 (online)
Publication History
Publication Date:
23 February 2010 (online)
Abstract
Synthesis of 5-epi-(-)-hyacinthacine A3 and (-)-hyacinthacine A3 has been achieved from the d-xylose-derived polyhydroxylated cyclic nitrone. Our synthetic strategy is potentially general and flexible for the synthesis of both epimers of 5-alkyl-hyacinthacines.
Key words
nitrone - α-amino nitrile - iminosugars - polyhydroxylated pyrrolizidine - hyacinthacine
- Supporting Information for this article is available online:
- Supporting Information
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References and Notes
The crystal structure of 19 has been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number: CCDC 756239.