Journal of the Chemical Society. Chemical communications p. 2213 - 2214 (1995)
Update date:2022-08-10
Topics:
Avalos, Martin
Babiano, Reyes
Cabanillas, Andres
Cintas, Pedro
Dianez, Maria J.
et al.
Thioisomuenchnones undergo 1,3-dipolar cycloaddition with chiral nitroalkenes to afford stereoselectively 4,5-dihydrothiophenes by means of an unprecedented fragmentation of cycloadducts; the structures of these products have been established by single cr
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