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Boulton-Katritzky rearrangement mechanism

A theoretical study of degenerate Boulton-Katritzky rearrangements concerning the anions of 3-formylamino-l,2,4-oxadiazole and 3-hydroxy-iminomethyl-1,2,5-oxadiazole has been carried out7 The treatment has shown the participation of asymmetric transition states and non-concerted processes via symmetrical intermediates. A detailed ab initio and density functional study of the Boulton-Katritzky rearrangement of 4-nitrobenzofuroxan has indicated a one-step mechanism for the process. [Pg.504]

Based on numerous mechanistic studies, the mechanism of the bicyclic Boulton-Katritzky rearrangement can be generalized as follows ... [Pg.528]

See other pages where Boulton-Katritzky rearrangement mechanism is mentioned: [Pg.34]    [Pg.37]    [Pg.245]    [Pg.318]    [Pg.238]    [Pg.482]    [Pg.534]    [Pg.37]    [Pg.40]    [Pg.570]    [Pg.14]   
See also in sourсe #XX -- [ Pg.528 ]



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Boulton-Katritzky

Mechanism rearrangement

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