LIGULAVERIN-A, A STRUCTURALLY NOVEL SESQUITERPENOID-DERIVED METABOLITE POSSIBLY FORMED VIA A BIOLOGICAL DIELS-ALDER REACTION

Authors
ZHAO Y PARSONS S BAXTER RL JIA ZJ SUN HD RANKIN DWH
Citation
Y. Zhao et al., LIGULAVERIN-A, A STRUCTURALLY NOVEL SESQUITERPENOID-DERIVED METABOLITE POSSIBLY FORMED VIA A BIOLOGICAL DIELS-ALDER REACTION, Chemical communications, (21), 1996, pp. 2473-2474
Citations number
5
Categorie Soggetti
Chemistry
Journal title
Chemical communications → ACNP
ISSN journal
13597345
Issue
21
Year of publication
1996
Pages
2473 - 2474
Database
ISI
SICI code
1359-7345(1996):21<2473:LASNSM>2.0.ZU;2-E
Abstract
The crystal structure of Ligulaverin A 1, isolated from Ligularia veit chiana (Hemsl,) Greenm,, reveals a novel carbocyclic skeleton which is likely to be derived from a hydroxymethacrylate ester of an eremophil ane sesquiterpenoid via an intramolecular Diels-Alder reaction.