作者:Michiko Tamano、Jugo Koketsu
DOI:10.1246/bcsj.58.2577
日期:1985.9
addition of diethyl disulfide gave the reduction products of the ketones and S,S-diethyl phenylphosphonodithioate or S,S-diethyl phenylphosphonotrithioate. A possible intermediate of the phosphine moiety was suggested to be phenylphosphinylidene [PhP=O] or phenylphosphinothioylidene [PhP=S]. The reduction of 10,10′-bianthrone and Δ10,10′-bianthrone resulted in the cleavage of the carbon–carbon single and double
某些芳族酮或硫酮与苯基膦反应并随后加入二乙基二硫化物得到酮和 S,S-二乙基苯基二硫代膦酸酯或 S,S-二乙基苯基膦酰三硫代酯的还原产物。膦部分的可能中间体被认为是苯基亚膦基[PhP=O]或苯基亚膦硫基[PhP=S]。10,10'-联蒽酮和Δ10,10'-联蒽酮的还原分别导致碳-碳单键和双键的断裂和羰基的还原。