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Wiehler isoxazole synthesis

Isoxazoles from condensation of aryl aldehydes and a-nitro-esters. Interestingly, the nitrogen atom at the isoxazole ring comes from the nitro group. [Pg.120]

Cr(CO)3-coordinated hydroquinone from vinylic alkoxy pentacarbonyl chromium carbene complex (Fischer carbene) and alkynes. [Pg.122]

In Advances in Metal-Organic Chemistry Liebeskind, L. S., Ed. JAI Press, Greenwich, CT 1989 Vol. 1. (Review). [Pg.122]

Torrent, M. Catalysis Metal Complexes 2002, 25, 269. [Pg.122]

Radical-mediated ring expansion of 2-haIomethyl cycloalkanones. [Pg.123]


See other pages where Wiehler isoxazole synthesis is mentioned: [Pg.249]    [Pg.1125]    [Pg.120]    [Pg.107]    [Pg.249]    [Pg.1125]    [Pg.120]    [Pg.107]   


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Isoxazole synthesis

Isoxazoles synthesis

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