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Arynes and heteroarynes

Arynes and heteroarynes are reactive intermediates derived formally by the removal of two adjacent hydrogens from, respectively, a carbocyclic or a heterocyclic aromatic ring. Prototypical examples are benzyne (1) and 3,4-didehydropyridine (2). Since these molecules contain a partial triple bond, they are properly regarded as -ynes and, as will be seen, undergo many reactions typical of that functionality, modified by the inherent strain caused by their nonlinearity. [Pg.1018]


See other pages where Arynes and heteroarynes is mentioned: [Pg.24]    [Pg.141]    [Pg.24]    [Pg.1017]    [Pg.1019]    [Pg.1021]    [Pg.1023]    [Pg.1025]    [Pg.1027]    [Pg.1029]    [Pg.1031]    [Pg.1033]    [Pg.1037]    [Pg.1039]    [Pg.1041]    [Pg.1043]    [Pg.1045]    [Pg.1047]    [Pg.1049]    [Pg.1051]    [Pg.1053]    [Pg.1055]    [Pg.1057]    [Pg.1059]    [Pg.1061]    [Pg.1063]    [Pg.1065]    [Pg.1067]    [Pg.1069]    [Pg.1071]    [Pg.1073]    [Pg.1075]    [Pg.1077]    [Pg.1079]    [Pg.1081]    [Pg.1083]    [Pg.1085]    [Pg.1087]    [Pg.1091]    [Pg.1093]    [Pg.1095]    [Pg.1097]    [Pg.1099]    [Pg.1101]    [Pg.1103]    [Pg.1105]    [Pg.1107]    [Pg.1109]    [Pg.1111]    [Pg.1113]   
See also in sourсe #XX -- [ Pg.225 ]




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Aryne

Heteroarynes

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