6533b859fe1ef96bd12b76cc

RESEARCH PRODUCT

1H and 13C NMR signal assignment of synthetic (-)-methyl thyrsiflorin B acetate, (-)-thyrsiflorin C and several scopadulane derivatives.

Miguel A. GonzálezRamón J. Zaragozá

subject

Methyl thyrsiflorin B acetateCarbon IsotopesMagnetic Resonance SpectroscopyStereochemistryChemistryMolecular ConformationStereoisomerismGeneral ChemistryCarbon-13 NMRDEPTReference StandardsSignalThyrsiflorin CProton NMRGeneral Materials ScienceDiterpenesProtonsSpectroscopy

description

The 1H and 13C NMR signal assignment of the data of 13 scopadulane-type diterpenes is reported. It was based on one- and two- dimensional NMR techniques which included 1H, 13C, DEPT, HMQC and 1D NOE difference spectroscopy. Copyright © 2005 John Wiley & Sons, Ltd.

10.1002/mrc.1629https://pubmed.ncbi.nlm.nih.gov/16106476