-
[文献書誌] Otera. J. et al.: "Diastereocontrol in Lewis acid-catalyzed Michael reactions of 4-siloxycyclopentenone with ketene silvl acetals: stereoelectronic vs. steric effect" Tetrahedron Lett.36. 95-98 (1995)
-
[文献書誌] Fukuzumi, S.: Okamoto, T.; Fujita, M: Otera, J.: "Importance of steric hindrance in Iinear coordination of Lewis acids with a-enones" J. Chem. Soc., Chem. Commun.(in press.).
-
[文献書誌] Fujita, M.; Fukuzumi, S.; Matsubayashi, G.: Otera, J.: "Preference of electron transfer to polar pathway in addition of ketene silyl acetals with quinones and catalysis of magnesium ion" Bull. Chem. Soc. Jpn.(in press.).
-
[文献書誌] Otera, J., Fujita. Y.: Sakuta, N.; Fujita, M.: Fukuzumi. S.: "Mechanism of Mukaivama-Michael reaction of ketene silyl acetal: electron transfer of nucleophilic addition?" J. Org. Chem.(in press.).
-
[文献書誌] Otera. J.; Chen, J.: "Unprecedented preference for aldehyde over acetal over acetal in organotin Lewis acid-promoted Mukaiyama-aldol reaction of ketene silyl acetals" Synlett. (in press.).
