30829-30-2Relevant articles and documents
Reaction of esters of PIII acids with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone
Gazizov,Ismagilov,Shamsutdinova,Tarakanova,Karimova
, p. 2943 - 2947 (2017/06/05)
A reaction of PIII acid esters with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone leads to the formation of phosphorylated phosphorus ylides, 3,3’,5,5’-tetra-tert-butylstilbenequinone, and diphosphorylated sterically hindered phenols. The schemes for the formation of these products through the primary key intermediates of betaine and phosphorus ylide structures were suggested.
Method for producing benzylidene derivatives
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, (2008/06/13)
A selective and high-yield method is described for producing stereoisomeric benzylidene derivatives of the formula III: STR1 wherein R1 and R2 each independently is lower alkyl, lower alkoxy or halogen; Y is SO2, SO or CO;