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<jats:p> Ma <jats:italic>et al</jats:italic> . (Reports, 10 October 2014, p. 219) report asymmetric syntheses of sceptrin and massadine and, through a stereochemical reassignment, claim to “uncover enantiodivergence as a new biosynthetic paradigm for natural products.” We challenge and clarify this claim with relevant examples from the literature of this well-known phenomenon of enantiodivergent congener biosynthesis within the same producing organism. </jats:p>

<jats:p> Sherman <jats:italic>et al</jats:italic> . commented on the precedence of enantiodivergence, listing a number of congeneric natural products with opposite chirality. However, these “congeners” are not derived from enantiodivergent biosyntheses. Instead, they are antipodes arising from separate enantiomeric biosyntheses. A distinct feature of the biosynthesis of the cyclic pyrrole-imidazole dimers is the production of antipodal congeners without the corresponding enantiomers. </jats:p>