A formal total synthesis of (-)-dysiherbaine

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A key intermediate hexahydrofuropyran 2 to (-)-dysiherbaine 1 has been synthesized concisely via intramolecular oxymercuration and iodocyclization to install the asymmetric centers at the ring junction and the amino group in the tetrahydropyran stereoselectively.
Publisher
GEORG THIEME VERLAG KG
Issue Date
2003-06
Language
English
Article Type
Article
Keywords

SPONGE DYSIDEA-HERBACEA; AMINO-ACID RECEPTORS; NERVOUS-SYSTEM; DOMOIC ACID; GLUTAMATE; EXCITOTOXICITY; DYSIHERBAINE; NEUROPATHOLOGY; NEUROTOXICITY; PHARMACOLOGY

Citation

SYNLETT, v.23, no.7, pp.993 - 994

ISSN
0936-5214
URI
http://hdl.handle.net/10203/78997
Appears in Collection
CH-Journal Papers(저널논문)
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