A formal total synthesis of (-)-dysiherbaine

Cited 27 time in webofscience Cited 0 time in scopus
  • Hit : 395
  • Download : 0
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)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 27 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0