Chemistry of Heterocyclic Compounds p. 1367 - 1369 (1986)
Update date:2022-08-04
Topics:
Golubev, A. A.
Semenenko, M. N.
Mandrugin, A. A.
Fedoseev, V. M.
Depending on the conditions employed, thiourea reacts with the hydrobromide of 2-bromo-3-aminopropionic acid to give a dihydrobromide of an internal salt S-(2-amino-1-carboxyethyl)isothiourea.This compound can also lose ammonia to give a thiazoline derivative.
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Doi:10.1016/S0020-1693(00)81239-6
(1987)Doi:10.1246/cl.1986.1627
(1986)Doi:10.1246/cl.1987.29
(1987)Doi:10.1016/j.bmcl.2008.10.115
(2009)Doi:10.1134/S1070363216050327
(2016)Doi:10.1021/acs.orglett.9b01338
(2019)
