On the reactions of benzeneseleninic anhydride with monosubstituted hydrazones. Evidence for radical pathways.
作者:Derek H.R. Barton、Takashi Okano、Shyamal I. Parekh
DOI:10.1016/s0040-4020(01)96097-1
日期:1991.3
The known oxidation of mono-substituted hydrazones by benzeneseleninicanhydride has been studied using 77Se and 13C NMR spectroscopy. The intermediates in the reaction have been identified. Good evidence that certain steps in these reactions are radical in character has been secured.
使用77 Se和13 C NMR光谱研究了已知的苯硒酸酐对单取代的氧化反应。已经确定了反应中的中间体。这些反应中某些步骤本质上是激进的,已经得到了充分的证据。
PROCESS FOR SYNTHESIS OF ORGANOMETALLIC COMPOUNDS
申请人:SEKISUI CHEMICAL CO., LTD.
公开号:EP1431302B1
公开(公告)日:2009-03-18
Convenient Route to Fischer-Type Carbene Ruthenium Complexes: Highly Selective Catalysts for Ring Opening/Cross-Metathesis of Norbornene Derivatives
作者:Hiroyuki Katayama、Masato Nagao、Fumiyuki Ozawa
DOI:10.1021/om020772z
日期:2003.2.1
The Fischer-type ruthenium carbene complexes RuCl2=C(H)ER}(PCy3)(2) (ER = SPh (1a), SC6H4Me-p (1b), SC6H4Cl-p (1c), SC6H4OMe-p (1d), SePh (1e)) have been prepared by the reactions of Ru(p-cymene)(cod), PCy3, and the corresponding dichloromethyl chalcogenides (Cl2CHER) in 47-80% yields. The starting Ru(p-cymene)(cod) is readily synthesized in high yield from [RuCl2(p-cymene)](2). The X-ray structures of 1b and 1e are reported. Complexes la and le serve as highly selective catalysts for ring opening/cross-metathesis of norbornene derivatives with vinyl chalcogenides.
A Convenient Synthesis of Arylselenoacetals and α-Halo-α-(phenylseleno)alkanes
作者:Claudio C. Silveira、Gelson Perin、Antonio L. Braga
DOI:10.1080/00397919508010797
日期:1995.1
alpha-Halo-alpha-(phenylseleno)alkanes are prepared by treatment of selenoacetals with halogenating agents. Selenoacetals are produced by heating alpha-halo-alpha-(phenylseleno)alkanes on neutral alumina