Yan Jiangli, Kline Allen D, Mo Huaping, Shapiro Michael J, Zartler Edward R
Discovery Chemistry Research and Technologies, Lilly Research Labs, Lilly Corporate Center, Eli Lilly & Company, Indianapolis, Indiana 46285, USA.
J Org Chem. 2003 Mar 7;68(5):1786-95. doi: 10.1021/jo020670i.
A novel method for the determination of the relative stereochemistry of six-membered chairlike ring molecules by residual dipolar couplings is presented. C-H residual dipolar couplings were used to investigate the relative stereochemistry of 4,6-O-ethylidene-d-glucopyranose. For this and similar systems it is not necessary to acquire redundant dipolar couplings and to calculate the orientation order tensor. The presented methodology is a paradigmatic leap for the determination of the relative stereochemistry or remote stereochemistry in this kind of fused ring system. Residual dipolar coupling data were collected by 1D and 2D direct-measurement heteronuclear multiple quantum coherence (HMQC) spectroscopy. It was demonstrated that direct measurement of HMQC was quick and accurate for small molecules at natural abundance.
本文提出了一种通过残余偶极耦合来测定六元椅状环分子相对立体化学的新方法。利用C-H残余偶极耦合研究了4,6-O-亚乙基-d-吡喃葡萄糖的相对立体化学。对于该体系及类似体系,无需获取冗余的偶极耦合并计算取向序张量。所提出的方法在这类稠环体系中相对立体化学或远程立体化学的测定方面是一个范式性的飞跃。残余偶极耦合数据通过一维和二维直接测量异核多量子相干(HMQC)光谱收集。结果表明,对于天然丰度下的小分子,HMQC的直接测量快速且准确。