SYNTHESIS OF NOVEL CROWN ETHER INCORPORATING THE (−)-(5<i>S</i>,6<i>R</i>,13<i>S</i>,14<i>R</i>)-5,6,13,14-TETRAHYDRO-5,13-METHANOCYCLOOCTA[1,2-<i>a</i>:5,6-<i>a</i>′]DINAPHTHALENE-6,14-DIOL SUBUNIT AS THE C<sub>2</sub>-SYMMETRIC CHIRAL CENTER
作者:Koichiro Naemura、Rinko Fukunaga
DOI:10.1246/cl.1985.1651
日期:1985.11.5
(−)-5,6,13,14-Tetrahydro-5,13-methanocycloocta[1,2-a:5,6-a′]dinaphthalene-6,14-diol was synthesized and its absolute configuration was established. Optically active crown ether was prepared by using this glycol as a source of chirality and its chiral recognition property was examined.
(-)-5,6,13,14-Tetrahydro-5,13-methanocycloocta[1,2-a:5,6-a']dinaphthalene-6,14-diol 被合成并确定其绝对构型。以该二醇为手性源制备了旋光冠醚并考察了其手性识别性能。