Taxonomy: Physicochemical and Pharmacological Properties of Sesquiterpene Esters – The Bicyclic Sesquiterpene Esters – Eremophilanes – Furanoeremophilanes – Diesters
Biological sources: Othonna natalensis Sch. Bip. [1]; O. leptodactyla Harv. [2]; Hertia pallens Kuntze. [3]
C25H34O7: 446.2305
Mp: colorless oil [1]
IR (CCl4): 1735, 1720, 1650 [1]
MS: 446.230 [M]+ (1) (calc. for C25H34O7 446.230, 358 (12), 83 (100) [1]
1 H NMR (270 MHz, CDCl3): 0.99 (3H, s, H-14), 2.25 (1H, m, H-10), 2.30 (1H, br d, J = 17, H-9b), 2.92 (1H, dd, J = 17; 8, H-9a), 2.99 (1H, d, J = 5, H-4), 5.50 (1H, ddd, J = 10; 5; 5, H-3), 6.33 (1H, s, H-6), 6.31 (1H, br s, H-2″ in OiBu), 6.41 (1H, br s, H-3′ in OAng) [1]
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
F. Bohlmann, K.-H. Knoll, Phytochemistry 17(3), 461 (1978)
J. Jakupovic, V.P. Patnak, M. Grenz, S. Banerjee, C. Wolfrum, R.N. Baruah, F. Bohlmann, Phytochemistry 26(4), 1049 (1987)
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-6β-isobutyroyloxy-10βH-furanoeremophilan-15-oic Acid Methyl Ester. In: Azimova, S.S., Saidkhodzhaev, A.I. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0539-9_1357
Download citation
DOI: https://doi.org/10.1007/978-1-4614-0539-9_1357
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