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1H and 13C resonance designation of antimycin A1 by two-dimensional NMR spectroscopy

January 1, 1987

Complete 1H and 13C resonance assignments of antimycin A1 were accomplished by two-dimensional NMR techniques, viz. 1H homonuclear COSY correlation, heteronuclear 13C-1H chemical shift correlation and long-range heteronuclear 13C-1H COLOC correlation. Antimycin A1 was found to consist of two isomeric components in a 2:1 ratio based on NMR spectroscopic evidence. The structure of the major component was newly assigned as the 8-isopentanoic acid ester. The spectra of the minor component were consistent with the known structure of antimycin A1.

Publication Year 1987
Title 1H and 13C resonance designation of antimycin A1 by two-dimensional NMR spectroscopy
DOI 10.1002/mrc.1260251212
Authors S. L. Abidi, B.R. Adams
Publication Type Article
Publication Subtype Journal Article
Series Title Magnetic Resonance in Chemistry
Index ID 70006653
Record Source USGS Publications Warehouse
USGS Organization Upper Midwest Environmental Sciences Center