COMPLETE H-1 AND C-13 NMR SPECTRAL ASSIGNMENT OF PENTACYCLO [6.4.0.0(2,6).0(5,9).0(4,12)]DODECANE DERIVATIVES AND STRUCTURE ELUCIDATION OF PENTACYCLO [6.4.0.0(2,6).0(3,11).0(5,9)]DODECANE

Authors
MARTINS FJC COETZEE GH FOURIE L VENTER HJ VILJOEN AM WESSELS PL
Citation
Fjc. Martins et al., COMPLETE H-1 AND C-13 NMR SPECTRAL ASSIGNMENT OF PENTACYCLO [6.4.0.0(2,6).0(5,9).0(4,12)]DODECANE DERIVATIVES AND STRUCTURE ELUCIDATION OF PENTACYCLO [6.4.0.0(2,6).0(3,11).0(5,9)]DODECANE, Magnetic resonance in chemistry, 31(6), 1993, pp. 578-584
Citations number
18
Categorie Soggetti
Spectroscopy,Chemistry
Journal title
Magnetic resonance in chemistry → ACNP
ISSN journal
07491581
Volume
31
Issue
6
Year of publication
1993
Pages
578 - 584
Database
ISI
SICI code
0749-1581(1993)31:6<578:CHACNS>2.0.ZU;2-1
Abstract
Treatment of entacyclo[6,4.0.0(2.6).0(5.9).0(4,12)]dodecan-2-ol with c oncentrated sulphuric acid produced the rearranged hydrocarbon pentacy clo[6.4.0.0(2,6).0(3,11).0(5,9)]dodecane as the main product. High-fie ld H-1 and C-13 NMR techniques were used in the structure elucidation and assignment of the different NMR resonances of these two and relate d compounds.