Taxonomy: Physicochemical and Pharmacological Properties of Sesquiterpene Esters – The Bicyclic Sesquiterpene Esters – Eremophilanes – Furanoeremophilanes – Monoesters
Biological sources: Othonna quinquedentata Thunb. [1]; O. triplinervia DC. [2]; Hertia pallens Kuntze. [3]
C20H26O4: 330.4070
MS: 330 [M]+ (12), 247 (0.3), 230 (5), 83 (45), 55 (100) [1]
1 H NMR (100 MHz, C6D6): 1.37 (3H, s, H-14), 2.00 (3H, d, J = 1, H-13), 2.55 (2H, m, H-9), 3.68 (1H, dd, J = 11; 7.5, H-15β), 3.91 (1H, dd, J = 7.5; 7.5, H-15α), 4.57 (1H, br s, H-6), 5.31 (1H, dd, J = 5; 2, H-3), 7.00 (1H, q, J = 1, H-12); OAng: 1.79 (3H, dq, J = 1; 1, (in CDCl3 m), H-5′), 1.95 (3H, dq, J = 7; 1 (in CDCl3 m), H-4′), 5.75 (1H, qq, J = 7; 1, (in CDCl3 m), H-3′) [1]
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsReferences
F. Bohlmann, N. Rao, Tetrahedron Lett. 14, 613 (1973)
F. Bohlmann, K.-H. Knoll, Phytochemistry 17(3), 461 (1978)
J. Jakupovic, F. Bohlmann, M. Grenz, Phytochemistry 28(11), 3231 (1989)
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media New York
About this entry
Cite this entry
(2013). 3β-Angeloyloxy-6,15-epoxy-furanoeremophilane. In: Azimova, S.S., Saidkhodzhaev, A.I. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0539-9_1122
Download citation
DOI: https://doi.org/10.1007/978-1-4614-0539-9_1122
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4614-0538-2
Online ISBN: 978-1-4614-0539-9
eBook Packages: Chemistry and Materials ScienceReference Module Physical and Materials ScienceReference Module Chemistry, Materials and Physics