Article ID Journal Published Year Pages File Type
5217484 Tetrahedron 2013 6 Pages PDF
Abstract

The configuration of (−)-brevianamides was assigned as (2S,13S) based on X-ray structure analysis and hydrolysis experiments. However, our theoretical investigation of its chiroptical properties strongly implied that the correct configuration should be (2R,13R). The reasons for the incorrect earlier assignment are analyzed by calculations of conversion energy barriers among different intermediates, starting materials and final products. This study demonstrates that conflicting theoretical and, experimental results suggest that it is premature to assign the configuration of a natural product.

Graphical abstractTransition state computations were performed for the conversion at the B3LYP/6-311++G(2d,p) level.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry