作者:A.C. Bellaart
DOI:10.1016/s0040-4020(01)96949-2
日期:1965.1
The reduction of 1- and 2-nitronaphthalene and of some mono- and dinitro-biphenyls with phosphine was carried out under the conditions described by Buckler.1 Reduction of 1-nitro-naphthalene did not yield any crystalline product while reduction of 2-nitronaphthalene yielded benzo[f]naphtho[2,1-c]cinnoline-N-oxide together with 2,2′-azoxynaphthalene. The mononitro-biphenyls and 4,4′-dinitrobiphenyl were
在Buckler描述的条件下,用膦还原1-和2-硝基萘以及一些单-和二硝基-联苯。1还原1-硝基萘不会生成任何结晶产物,而还原2-硝基萘则会生成苯并[f]萘并[2,1-c]萘啉-N-氧化物与2,2'-氮氧基萘。单硝基联苯和4,4'-二硝基联苯很容易还原为a氧基化合物,而2,2'-二硝基联苯的还原则生成苯并[c] cinnoline-N,N'-二氧化物。