-
[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 Leff.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, ; Fukuzumin, S. ; Matsubayashi, G. ; Otera, J.: "Preferene of electron transfer to polar pathway in addition of ketene silvl 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 Mukaiyama-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 in organotin Lewis acid-promoted Mukaiyama-aldol reaction of ketene silyl acetals" Synlett. (in press.).
