ORGANIC SYNTHESIS. Response to Comment on "Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence"
- PMID: 26160939
- PMCID: PMC4536548
- DOI: 10.1126/science.aaa9626
ORGANIC SYNTHESIS. Response to Comment on "Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence"
Abstract
Sherman et al. 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.
Copyright © 2015, American Association for the Advancement of Science.
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Comment on
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Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence.Science. 2014 Oct 10;346(6206):219-24. doi: 10.1126/science.1255677. Science. 2014. PMID: 25301624 Free PMC article.
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ORGANIC SYNTHESIS. Comment on "Asymmetric syntheses of sceptrin and massadine and evidence for biosynthetic enantiodivergence".Science. 2015 Jul 10;349(6244):149. doi: 10.1126/science.aaa9349. Epub 2015 Jul 9. Science. 2015. PMID: 26160938 Free PMC article.
References
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