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2.6- Lutidinium perchlorate

An interesting application of the electrochemical oxidation of thiocyanate ion is the preparation of alkyl and aryl thiocyanates via anodically generated thiocyanogen. Alcohols have been converted to the corresponding thiocyanates by constant current electrolysis of NaSCN in CH2CI2 containing triphenylphosphite and 2,6-lutidinium perchlorate. The yields were fair to good for the primary and secondary alcohols, but no thiocyanate formation was observed with tertiary ones. Similarly, various aromatic amines and phenols were thiocyanated in a two-step procedure, namely electrochemical preparation of (SCN)2 and subsequent reaction with the substrates k... [Pg.620]

Comb-like derivatives of amylose have been prepared by condensation of l,2-(t-butyl orthoacetate) and l,2-(ethyl orthoacetate) derivatives of 3,4,6-tri-O-acetyl-a-D-glucopyranose with 2,3-di-O-phenylcarbamoyl derivatives of amylose in boiling chlorobenzene in the presence of 2,6-lutidinium perchlorate as catalyst. The distance between the branch points, attached mainly by(l- -6)-j3-D- with a small proportion of (l->6)-a-D-linkages as indicated by n.m.r. [Pg.539]

Abbreviations Ac acetyl Bn benzyl BSP 1-benzenesulfinyl piperidine BTIB bis(trifluoroacetoxy)iodobenzene DAST (diethylamino)sulfur trifluoride DDQ 2,3-dichloro-5,6-dicyano-/)-benzoquinone DMDO dimethyldioxirane DMTSF dimethyl(methylthio)sulfonium tetrafluoroborate DMTST dimethyl(methylthio)sulfonium triflate DTBMP 2,6-Ai-tert-butyl-4-methylpyridine DTBP 2,6-di-tert-butylpyridine DTBPl 2,6-di-tert-butylpyridinium iodide FDCPT l-fluoro-2,6-dichloropyridinium triflate FTMPT l-fluoro-2,4,6-trimethylpyridinium triflate IDCP iodonium dicollidine perchlorate IDCT idonium dicollidine triflate LPTS 2,6-lutidinium p-toluenesulfonate LTMP lithium tetramethylpiperidide Me methyl MPBT S-(4-methoxyphenyl) benzenethiosulflnate NBS A-bromosuccinimide NIS A-iodosuccinimide NlSac A-iodosaccharin PPTS pyridinium p-toluenesulfonate TBPA tris(4-bromophenyl)ammoniumyl hexachloroantimonate Tf trifluoromethanesulfonyl TMTSB methyl-bis(methylthio)sulfonium hexachloroantimonate TMU tetramethylurea Tr trityl TTBP 2,4,6-tri-tert-butylpyrimidine. [Pg.109]


See other pages where 2.6- Lutidinium perchlorate is mentioned: [Pg.256]    [Pg.272]    [Pg.128]    [Pg.256]    [Pg.256]    [Pg.272]    [Pg.128]    [Pg.256]   


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Lutidinium

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