Conclusions
The opening of the oxide ring of the diethyl acetal of epoxybutyraldehyde by ammonia or benzylamine goes selectively both structurally and sterically, with the formation of o-hydroxy-β-amino compounds of the erythro series.
This is a preview of subscription content, log in via an institution to check access.
Literature cited
L. A. Yanovskaya, B. I. Kozyrkin, and V. F. Kucherov, Izv. AN SSSR, Ser. Khim.1966, 683.
H. J. Shine and J. Y.-F. Tsai, J. Organ. Chem.29, 443, 1964.
Y. Liwschitz, A. Singerman, and M. Luwish, Israel. J. Chem.1, No. 4, 441 (1963); C. A.60, 13121 (1964).
M. P. Berry and M. G. Whiting, J. Chem. Soc.1964, 862.
B. Palmeta and M. Prostenik, Tetrahedron19, 1463 (1963).
Author information
Authors and Affiliations
Additional information
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 919–920, May, 1966.
Rights and permissions
About this article
Cite this article
Kozyrkin, B.I., Yanovskaya, L.A. & Kucherov, V.F. Reaction of epoxybutyraldehyde diethyl acetal with ammonia and benzylamine. Russ Chem Bull 15, 876–877 (1966). https://doi.org/10.1007/BF00849391
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00849391