Using empirical rules from 13C NMR analysis to determine the stereochemistry of the epoxide located at the 5,6-position of decalinic systems

Raquel M. Cravero; Guillermo R. Labadie; Manuel Gonzalez Sierra

Conference ProceedingsOPEN ACCESS

Using empirical rules from 13C NMR analysis to determine the stereochemistry of the epoxide located at the 5,6-position of decalinic systems

Molecules (2000) 5(3) 323-324

DOI: 10.3390/50300323

2Citations

5Readers

Abstract

An empiric rule derived from the analysis of the 13C NMR spectral data, allowed us to determine 5,6-epoxide stereochemistry on decalinic systems and a discussion of the scope and limitations of this rule and its extension to other carbon squeletons, is presented.

Cite

CITATION STYLE

APA

Cravero, R. M., Labadie, G. R., & Gonzalez Sierra, M. (2000). Using empirical rules from 13C NMR analysis to determine the stereochemistry of the epoxide located at the 5,6-position of decalinic systems. In Molecules (Vol. 5, pp. 323–324). Molecular Diversity Preservation International. https://doi.org/10.3390/50300323

Using empirical rules from 13C NMR analysis to determine the stereochemistry of the epoxide located at the 5,6-position of decalinic systems

Abstract

Cite

Register to see more suggestions