PubMed · 17132003
Solid-phase total synthesis and structure proof of callipeltin B.
Abstract
The cytotoxic, cyclic heptadepsipeptide, natural product callipeltin B was synthesized on a solid-phase support in 15% overall yield. Comparison of the 1H NMR spectra of three synthetic isomers with those of callipeltin B confirmed the configurational reassignment of its threonine residues as d-allothreonine and the assignment of the configuration of its beta-methoxytyrosine residue as (2R,3R).
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Ravi Krishnamoorthy, Leslie D Vazquez-Serrano, Jeffrey A Turk, Jennifer A Kowalski, Alan G Benson, Nneka T Breaux, Mark A Lipton. 2006-12-06. Solid-phase total synthesis and structure proof of callipeltin B.. https://doi.org/10.1021/ja0666250
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