Hong Liang, Wang Lei, Sun Wangsheng, Wong Kwokyin, Wang Rui
State Key Laboratory of Applied Organic Chemistry and Institute of Biochemistry and Molecular Biology, Lanzhou University, Lanzhou 730000, China.
J Org Chem. 2009 Sep 4;74(17):6881-4. doi: 10.1021/jo901409d.
An enantioselective Friedel-Crafts alkylation/cyclization cascade reaction of 1-naphthols and alpha,beta-unsaturated aldehydes promoted by diphenylprolinol ether has been developed. The method affords one-pot access to chiral and synthetically useful chromanes and dihydrobenzopyranes in high yields and enantioselectivities from readily available compounds. In addition, the addition/cyclization products could be afterward transformed to various natural products and biologically active derivatives. On the basis of the experimental results and the observed absolute configurations of the products, a plausible mechanism has been proposed to explain the origin of the activation and the asymmetric induction.
已开发出由二苯基脯氨醇醚促进的1-萘酚与α,β-不饱和醛的对映选择性傅克烷基化/环化串联反应。该方法能从易得的化合物出发,通过一锅法以高产率和对映选择性得到手性且具有合成用途的色满和二氢苯并吡喃。此外,加成/环化产物随后可转化为各种天然产物和生物活性衍生物。基于实验结果和所观察到的产物绝对构型,提出了一种合理的机理来解释活化作用和不对称诱导的起源。