5(4H)-Oxazolones 1 and milnchnones 3 are reacted with triphenylvinylphosphonium bromide 2a to give, through a cycloaddition reaction, pyrrole derivatives 4a-d and 7a-c unsubstituted at C-3 and C-4. The use of substituted vinylphosphonium salts 2b,c and dipoles 1 and 3 allows the isolation of 3-methylpyrroles 4e, f and 7d,e and 3-pyrrolecarboxylic acids 9a-c, respectively. The cycloaddition reactions proceed with high regionelectivity because of the positive interaction of phosphonium group of 2 and carbonyl group of dipoles 1 and 3.

5(4H)-oxazolones. Part XI. Cycloaddition reaction of oxazolones and munchnones to triphenylvinylphosphonium salts as synthetic equivalents of alkynes / F. Clerici, M.L. Gelmi, P. Trimarco. - In: TETRAHEDRON. - ISSN 0040-4020. - 54:21(1998), pp. 5763-5774.

5(4H)-oxazolones. Part XI. Cycloaddition reaction of oxazolones and munchnones to triphenylvinylphosphonium salts as synthetic equivalents of alkynes

F. Clerici
Primo
;
M.L. Gelmi
Secondo
;
P. Trimarco
Ultimo
1998

Abstract

5(4H)-Oxazolones 1 and milnchnones 3 are reacted with triphenylvinylphosphonium bromide 2a to give, through a cycloaddition reaction, pyrrole derivatives 4a-d and 7a-c unsubstituted at C-3 and C-4. The use of substituted vinylphosphonium salts 2b,c and dipoles 1 and 3 allows the isolation of 3-methylpyrroles 4e, f and 7d,e and 3-pyrrolecarboxylic acids 9a-c, respectively. The cycloaddition reactions proceed with high regionelectivity because of the positive interaction of phosphonium group of 2 and carbonyl group of dipoles 1 and 3.
Settore CHIM/06 - Chimica Organica
1998
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/181932
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