## Abstract ^13^C NMR Spectra for a series of 11 substituted cyclobutanes derived from photodimerization of benzocycloalkenes were recorded. Comparison of the carbon chemical shifts for the headโtoโhead and headโtoโtail __cis__โ__syn__โ__cis__ and __cis__โ__anti__โ__cis__ isomers reveals shielding
Carbon-13 NMR spectra of methylated cyclobutanes and ethyl cyclobutane-carboxylates
โ Scribed by Ernest L. Eliel; K. Michal Pietrusiewicz
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 334 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
Abstract
The ^13^C NMR spectra of cyclobutane and seven methylated homologs and of ethyl cyclobutanecarboxylate and five isomeric diethyl cyclobutanedicarboxylates are reported and substituent parameters for methyl groups in methylcyclobutanes are calculated. Of note is a sizeable and nearly configurationโindependent upfield shifting ฮณโeffect.
๐ SIMILAR VOLUMES
13C NMR signals were assigned for a series of C-6 rnethylated steroids related to 5 acholestane, and the substituent effect of methyl groups at C-6 on the shielding data is discussed.
## Abstract The carbonโ13 NMR spectra have been recorded for representatives of three previously unexamined classes of pentacyclic triterpenesโlupanes, fernanes and arboranes. In addition to the spectra of lupeol methyl ether, cylindrin and arundoin, the spectra of a number of other triterpene meth
Low-temperature 13C NMR spectral data have been obtained for equatorial and axial methyl-, ethyl-and isopropylcyclohexane using a high-temperature cryogenic trapping technique. -C chemical shiโฌt differences between major and minor conformations of each compound are discussed in terms of chemical shi