The Guaianolide 11βH,13-Dihydromicheliolide

Autor: Frank R. Fronczek, J. Castañeda-Acosta, N. H. Fischer
Rok vydání: 1996
Předmět:
Zdroj: Acta Crystallographica Section C Crystal Structure Communications. 52:1263-1266
ISSN: 0108-2701
DOI: 10.1107/s0108270195015435
Popis: The lactone ring of the guaianolide-class sesquiterpene lactone [3S-(3α,3aα,9α,9aα,9bβ)]-3a,4,5,7,8,9,9a,9b-octahydro-9-hydroxy-3,6,9-trimethylazuleno[4,5-b]furan-2(3H)-one, C 15 H 22 O 3 , is trans-fused to the seven-membered ring. Two molecules are present in the asymmetric unit ; they differ only slightly in conformation. The seven-membered ring is in the chair conformation, with the local mirror bisecting the double bond. The lactone is in the envelope conformation, while the other five-membered ring adopts the half chair. The two independent molecules form a hydrogen-bonded dimer, with O...O distances 2.907 (3) and 2.966 (2) A.
Databáze: OpenAIRE