Challenges in the assignment of relative and absolute configurations of complex molecules: computation can resolve conflicts between theory and experiment

Abstract The configuration of (−)-brevianamides was assigned as (2 S ,13 S ) 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 (2 R ,13 R ). 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.