## Abstract Treatment of pentacyclo[6.4.0.0^2,6^.0^5,9^.0^4,12^]dodecane‐2‐ol with concentrated sulphuric acid produced the rearranged hydrocarbon pentacyclo[6.4.0.0^2,6^.0^3,11^.0^5,9^]dodecane as the main product. High‐field ^1^H and ^13^C NMR techniques were used in the structure elucidation and
Complete assignment of the 1H and 13C NMR spectra of a pentacyclo [5.4.0.02,6.03,10.05,9]undecane derivative
✍ Scribed by D. H. Cadd; W. J. Feast; A. M. Kenwright; J. M. Say
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 575 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The production of compounds derived from intramolecular photocycloaddition reactions upon Diels–Alder adducts has received considerable attention, but assignment of the NMR spectra of the photoaddition products has proved problematic, rendering structural determination difficult. This paper reports the complete assignments of the proton and carbon NMR spectra of 11, 11‐dimethoxypentacyclo [5.4.0.0^2,6^.0^3,10^.O^5,9^] undecan‐8‐one and the assignment of the spectra of pentacyclo [5.4.0.0^2,6^.0^3,10^.0^5,9^] undecan‐8,11‐dione by analogy.
📜 SIMILAR VOLUMES
the independent rings which comprise the compound. I.r. and Raman spectra were recorded, and a vibrational analysis was performed on the spectral quantities. The standard thermodynamic properties in the ideal-gas state were calculated in the temperature range 100 K to 1000 K. The calculated standard
## Abstract NMR techniques cannot unambiguously distinguish between 11‐amino‐8‐hydroxypentacyclo[5.4.0.0^2, 6^.0^3, 10^.0^5, 9^]undecane‐8,11‐lactam and 8‐amino‐11‐hydroxypentacyclo[5.4.0.0^2, 6^.0^3, 10^.0^5, 9^]undecane‐8,11‐lactam, both of which are possible products during the reaction of penta
The 1 H and 13 C NMR spectra of a set of structurally related tricyclic quinones consisting of 4,4-dimethylanthracene-1,9,10(4H)-trione (1), 4,4,6,7-tetramethylanthracene-1,9,10(4H)-trione (2) and the regioisomers 4,4,5-(3), 4,4,6-(4), 4,4,7-(5) and 4,4,8trimethylanthracene-1,9,10(4H)-trione (6) wer
The regiosomeric quinones 5-acetyloxymethyl-4,4,8-trimethyl-( ) and 8-acetyloxymethyl-4,4,5trimethylanthracene-1,9,10(4H)-trione (6) were synthesized and their regiochemistry was assigned on the basis of the unambiguous structure elucidation of 9,10-dihydroxy-5-acetyloxymethyl-4,4,8-trimethyl-5,8-di