Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan.
Chem Commun (Camb). 2009 Oct 21(39):5850-2. doi: 10.1039/b910192f. Epub 2009 Aug 11.
Cu(I)-catalyzed anti-S(N)2'-type reduction of internal propargylic carbonates with hydrosilanes affords various di- and trisubstituted allenes with high regioselectivities; the reactions are compatible with functional groups and work efficiently for the synthesis of optically-active allenes.
铜(I)催化的内炔丙基碳酸酯与硅烷的反-S(N)2'-型还原反应以高区域选择性得到各种二取代和三取代的丙二烯;该反应与官能团兼容,并且有效地用于合成光学活性的丙二烯。