• Sia, C.L., and Horrecker, B.L., Biochem. Biophys. Res. Commun. , 31 : 731, (1968).
• Jiang, Q. et al.: Nongyao, 49, 257 (1993)
• Augustin, M. et al.: Wissen. Zeitsch., 25, 5 (1993)
• Hanafi, W.Z.A. et al.: Plast. Rub. Comp. Proc. Appl., 19, 175 (1993)
• Noma, K. et al.: Shik. Kyok., 36, 225 (1993)
• For thermal (2+2)-cycloaddition with allene at high temperature, see: Org. Synth. Coll., 5, 459 (1973).
• Also undergoes photochemical and thermal (2+2)-cycloadditions with alkenes. For reaction with 1-alkynes, see: Chem. Ber., 102, 3974 (1969).
•
For use in combination with Urea hydrogen peroxide adduct, L13940, to generate peroxymaleic acid in epoxidation and Baeyer-Villiger reactions, see: Heterocycles, 36, 1075 (1993). Peroxymaleic acid can also be generated in situ from maleic anhydride and 30% H2O2 in NMP, and has been found to be a very effective oxidant for conversion of sulfides to sulfoxides. For a study of stoichiometric and catalytic oxidations with this system, see: J. Org. Chem., 61, 5693 (1996).•
Reactive dienophile. For a review of its Diels-Alder reactions, see: Org. React., 4, 1 (1948). For examples, see: Org. Synth. Coll., 3, 807 (1955); 4, 890 (1963). For reaction with Danishefsky's diene (1-Methoxy-3-trimethylsiloxy-1,3-butadiene, L14672), see: Org. Synth. Coll., 7, 312 (1990).
腐蚀性 (C)
有害性 (X)
