The Reaction of Nitrosoalkane Dimers with Acid Halides
作者:Max A. Ribi、Emil H. White
DOI:10.1002/hlca.19750580116
日期:——
Nitrosoalkane dimers react with acid halides to yield α-halogeno-azoxy compounds with the substituent α to the oxygen-bearing nitrogen. In the presence of silver carbonate, the corresponding α-acyloxy-azoxy compounds are formed.
Beger, J.; Neumann, R., Journal fur praktische Chemie (Leipzig 1954), 1989, vol. 331, # 2, p. 354 - 360
作者:Beger, J.、Neumann, R.
DOI:——
日期:——
Oxidation of gem-chloronitroso- and vic-chloronitroso-alkanes and -cycloalkanes to respective chloronitro compounds by novel cetyltrimethylammonium hypochlorite reagent
作者:ABDULKARIM H A MOHAMMED、GOPALPUR NAGENDRAPPA
DOI:10.1007/s12039-011-0090-7
日期:2011.7
Cetyltrimethylammonium hypochlorite (CTAHC) is prepared and used as an oxidizing agent for nitroso group to nitro group. The gem-chloronitroso and vic-chloronitroso compounds are prepared respectively from ketoximes and olefins by reacting with NOCl generated in situ from chlorotrimethylsilane (TMSCl) and iso-amyl nitrite. CTAHC oxidizes gem-chloronitroso and vic-chloronitroso compounds to the corresponding