The stereochemical dependence of 13C chemical shifts in olean-12-enes and urs-12-enes as an aid to structural assignment
- 1 January 1974
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 15 (27), 2381-2384
- https://doi.org/10.1016/s0040-4039(01)92261-0
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Mass spectrometric identification of oleanolic and ursolic acidsJournal of Mass Spectrometry, 1973
- Acetonide formation from olean-12-ene-16α,28- and -16β, 28-diolsJournal of the Chemical Society, Chemical Communications, 1973
- Constituents of Dipterocarpaceae Resins. IV. Triterpenes of Shorea acuminata and S. resina-nigraAustralian Journal of Chemistry, 1972
- Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. I. Direct analysis of nonprotonated carbon centersJournal of the American Chemical Society, 1969
- Carbon-13 magnetic resonance. IX. MethylcyclohexanesJournal of the American Chemical Society, 1967
- Carbon-13 magnetic resonance. VII. Steric perturbation of the carbon-13 chemical shiftJournal of the American Chemical Society, 1967
- Mass Spectrometry in Structural and Stereochemical Problems. XXXII.1 Pentacyclic TriterpenesJournal of the American Chemical Society, 1963
- Terpenoids. XXIV.1 The Structure of the Cactus Triterpene Queretaroic AcidJournal of the American Chemical Society, 1956
- Terpenoids. VIII.1 The Structures of the Cactus Triterpenes Gummosogenin and Longispinogenin2,3Journal of the American Chemical Society, 1954
- Terpenoids. III.1 The Isolation of Erythrodiol, Oleanolic Acid and a New Triterpene Triol, Longispinogenin, from the Cactus Lemaireocereus longispinus2Journal of the American Chemical Society, 1953