TY - JOUR
T1 - Swietenolide diacetate from the seeds of Swietenia macrophylla
AU - Goh, Bey Hing
AU - Abdul Kadir, Habsah
AU - Abdul Malek, Sri Nurestri
AU - Ng, Seik Weng
N1 - Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010
Y1 - 2010
N2 - The title compound, C31H38O10 [systematic name: (R,4R,4aR,6aS,7R,8S,10R,11S)-methyl ,10-di-acet-oxy-4-(3-furyl)-4a,7,9,9- tetra-methyl-2,13-dioxo-1,4,4a,5,6,6a,7,8,9,10,11,12-dodeca-hydro-7, 11-methano-2H-cyclo-octa-[f][2]benzo-pyran-8-acetate], was isolated from the seeds of Swietenia macrophylla. The mol-ecule contains four six-membered rings connected together in the shape of a bowl; one of the inner rings adopts a twisted chair conformation owing to the carbon-carbon double bond. The furyl substitutent is connected to an outer ring, and it points away from the bowl cavity.
AB - The title compound, C31H38O10 [systematic name: (R,4R,4aR,6aS,7R,8S,10R,11S)-methyl ,10-di-acet-oxy-4-(3-furyl)-4a,7,9,9- tetra-methyl-2,13-dioxo-1,4,4a,5,6,6a,7,8,9,10,11,12-dodeca-hydro-7, 11-methano-2H-cyclo-octa-[f][2]benzo-pyran-8-acetate], was isolated from the seeds of Swietenia macrophylla. The mol-ecule contains four six-membered rings connected together in the shape of a bowl; one of the inner rings adopts a twisted chair conformation owing to the carbon-carbon double bond. The furyl substitutent is connected to an outer ring, and it points away from the bowl cavity.
UR - http://www.scopus.com/inward/record.url?scp=77953225934&partnerID=8YFLogxK
U2 - 10.1107/S1600536810017733
DO - 10.1107/S1600536810017733
M3 - Article
AN - SCOPUS:77953225934
SN - 1600-5368
VL - 66
SP - o1396
JO - Acta Crystallographica Section E: Structure Reports Online
JF - Acta Crystallographica Section E: Structure Reports Online
IS - 6
ER -