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Synthesis 2008(9): 1455-1459
DOI: 10.1055/s-2008-1072534
DOI: 10.1055/s-2008-1072534
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Norpandamarilactonines, Pandamarilactonines, and Pandanamine
Further Information
Received
9 January 2008
Publication Date:
27 March 2008 (online)
Publication History
Publication Date:
27 March 2008 (online)
Abstract
A facile route to naturally occurring (±)-norpandamarilactonines A and B, (±)-pandamarilactonines A-D, and pandanamine has been described from 3-methylfuran-2(5H)-one, with a reductive intramolecular aza-Michael-type addition as the key step.
Key words
3-methylfuran-2(5H)-one - condensation - intramolecular aza-Michael reaction - pandamarilactonines
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1a
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1b
Tan M. Philippine Medicinal Plants in Common Use: Their Phytochemistry and Pharmacology AKAP; Quezon City: 1980. -
1c
Many websites describe the occurrence and properties of P. amaryllifolius leaves.
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References
The stereochemical assignments of compounds 10, 14, 15, 17, and 18 are based on NMR parameters. [8]