REACTIVITY OF 3,3'-METHYLENEBIS(5-PHENYL)OXAZOLIDINE WITH UREA, THIOUREA AND CYANAMIDE - AN ALTERNATIVE MECHANISM FOR THE BETA-UREIDOALKYLATION OF 2-AMINO-1-PHENYLETHANOL

Authors
PEVARELLO P PINCIROLI V VARASI M
Citation
P. Pevarello et al., REACTIVITY OF 3,3'-METHYLENEBIS(5-PHENYL)OXAZOLIDINE WITH UREA, THIOUREA AND CYANAMIDE - AN ALTERNATIVE MECHANISM FOR THE BETA-UREIDOALKYLATION OF 2-AMINO-1-PHENYLETHANOL, Journal of heterocyclic chemistry, 31(4), 1994, pp. 1089-1091
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
31
Issue
4
Year of publication
1994
Pages
1089 - 1091
Database
ISI
SICI code
0022-152X(1994)31:4<1089:RO3WUT>2.0.ZU;2-7
Abstract
The title compound 1 reacts with urea, thiourea and cyanamide, yieldin g the corresponding 1,3,5-triazine-2-one 3a, -2-thione Sb and an N,N-d icyanobisaminal 4 derivative, respectively. An alternative mechanism f or this class of alpha-ureidoalkylations is proposed.