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Triethylborane, reductive coupling with

A Sml2-induced reductive cyclization of (V-(alkylketo)pyrroles provided an entry into medium ring 1,2-annelated pyrroles <06EJO4989>. An oxidative radical alkylation of pyrroles with xanthates promoted by triethylborane provided access to a-(pyrrol-2-yl)carboxylic acid derivatives <06TL2517>. An oxidative coupling of pyrroles promoted by a hypervalent iodine(III) reagent provided bipyrroles directly <060L2007>. [Pg.147]

See other pages where Triethylborane, reductive coupling with is mentioned: [Pg.376]    [Pg.181]    [Pg.162]    [Pg.225]    [Pg.129]    [Pg.186]    [Pg.135]    [Pg.92]    [Pg.155]    [Pg.710]    [Pg.301]   
See also in sourсe #XX -- [ Pg.155 ]



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