The cycloaddition of 3,5-dichloro-2,4,6-trimethylbenzonitriloxide to chiral tricarbonylchromium complexed styrenes proceeds with high stereoselectivity, thus offering a new synthetic route to optically active 3,5-disubstituted 4,5-dihydroisoxazoles.

Baldoli, C., Delbuttero, P., Maiorana, S., Zecchi, G., Moret, M. (1993). TRICARBONYLCHROMIUM COMPLEXATION AS STEREOSELECTIVE TOOL IN NITRILE OXIDE CYCLOADDITIONS TO STYRENES. TETRAHEDRON LETTERS, 34(15), 2529-2532 [10.1016/S0040-4039(00)60460-4].

TRICARBONYLCHROMIUM COMPLEXATION AS STEREOSELECTIVE TOOL IN NITRILE OXIDE CYCLOADDITIONS TO STYRENES

MORET, MASSIMO
1993

Abstract

The cycloaddition of 3,5-dichloro-2,4,6-trimethylbenzonitriloxide to chiral tricarbonylchromium complexed styrenes proceeds with high stereoselectivity, thus offering a new synthetic route to optically active 3,5-disubstituted 4,5-dihydroisoxazoles.
Articolo in rivista - Articolo scientifico
CYCLO-ADDITION; ASYMMETRIC INDUCTION; CHIRAL AUXILIARIES; 1,3-DIPOLAR; NITRONES; TRICARBONYLCHROMIUM ARENES; STEREOSELECTIVE CYCLOADDITION; NITRILE OXIDE; 4,5-DIHYDROISOXAZOLES
English
1993
34
15
2529
2532
none
Baldoli, C., Delbuttero, P., Maiorana, S., Zecchi, G., Moret, M. (1993). TRICARBONYLCHROMIUM COMPLEXATION AS STEREOSELECTIVE TOOL IN NITRILE OXIDE CYCLOADDITIONS TO STYRENES. TETRAHEDRON LETTERS, 34(15), 2529-2532 [10.1016/S0040-4039(00)60460-4].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/32898
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