| Literature DB >> 27346894 |
Heriberto Rivera1, Sachin Dhar1, James J La Clair1, Shiou-Chuan Tsai2, Michael D Burkart1.
Abstract
Polyketide biosynthesis engages a series of well-timed biosynthetic operations to generate elaborate natural products from simple building blocks. Mimicry of these processes has offered practical means for total synthesis and provided a foundation for reaction discovery. We now report an unusual intramolecular trans-amidation reaction discovered while preparing stabilized probes for the study of actinorhodin biosynthesis. This rapid cyclization event offers insight into the natural cyclization process inherent to the biosynthesis of type II polyketide antibiotics.Entities:
Keywords: Cyclization; Intramolecular reactions; Polyketide; Reaction mechanisms; Trans-amidation
Year: 2016 PMID: 27346894 PMCID: PMC4917018 DOI: 10.1016/j.tet.2016.01.062
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457