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2.6- Di-tert-butyl-4-methylpyridine DTBMP

Both AgOTf and AgSbF6 (10mol%) were the best catalysts for this transformation, and the reaction was conducted in the presence of an hindered base, 2,6-di-tert-butyl-4-methylpyridine (DTBMP). The azomethine ylide CC intermediate has been identified in a test reaction in the absence of DMAD, via mass spectrometry. The scope and limitations have been thoroughly studied for reaching pyrroloisoquinoline scaffold, which is a substructure of the lamellarin alkaloid family. [Pg.154]

Carboxybenzyl glycoside Tf20/2,6-di-tert-butyl-4-methylpyridine (DTBMP) 55-57... [Pg.144]

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- Di-tert-butyl-4-methylpyridine DTBMP is mentioned: [Pg.40]    [Pg.407]    [Pg.105]    [Pg.1647]    [Pg.248]    [Pg.112]    [Pg.103]    [Pg.1144]    [Pg.40]    [Pg.407]    [Pg.105]    [Pg.1647]    [Pg.248]    [Pg.112]    [Pg.103]    [Pg.1144]    [Pg.669]    [Pg.117]    [Pg.98]    [Pg.637]    [Pg.702]    [Pg.108]    [Pg.308]    [Pg.338]    [Pg.637]    [Pg.589]    [Pg.576]   
See also in sourсe #XX -- [ Pg.268 ]




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2.6- tert-butyl-4-methylpyridine

3.4- Di-tert.-butyl

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