Abstract

In addition to the known 1,5,9-epideoxyloganic acid and 1,5,9-epideoxyloganin, Nepeta grandiflora has provided four new iridoid glucosides: 6′- O -acetoacetyl-, 2′- O -methyl-, 4′- O -methyl-, and 6′- O -methyl-1,5,9-epideoxyloganic acid. Their structures were proved by 1 H and 13 C-NMR studies. The conformation of the molecules was studied by molecular modelling and 1 H NMR coupling constant analysis. The absolute configurations were supported by CD spectroscopy.

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