1994•Journal of Heterocyclic ChemistryRequires access

Reactivity of 3,3′‐methylenebis(5‐phenyl)oxazolidine with urea, thiourea and cyanamide. An alternative mechanism for the α‐ureidoalkylation of 2‐amino‐l‐phenylethanol

Paolo Pevarello, Vittorio Pinciroli, Mario Varasi

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Abstract

Abstract The title compound 1 reacts with urea, thiourea and cyanamide, yielding the corresponding 1,3,5‐triazine‐2‐one 3a, ‐2‐thione 3b and an N,N‐dicyanobisaminal 4 derivative, respectively. An alternative mechanism for this class of α‐ureidoaikylations is proposed.

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What this paper is about

Abstract The title compound 1 reacts with urea, thiourea and cyanamide, yielding the corresponding 1,3,5‐triazine‐2‐one 3a, ‐2‐thione 3b and an N,N‐dicyanobisaminal 4 derivative, respectively. An alternative mechanism for this class of α‐ureidoaikylations is proposed.

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Available abstract

Abstract The title compound 1 reacts with urea, thiourea and cyanamide, yielding the corresponding 1,3,5‐triazine‐2‐one 3a, ‐2‐thione 3b and an N,N‐dicyanobisaminal 4 derivative, respectively. An alternative mechanism for this class of α‐ureidoaikylations is proposed.

Key concepts: Cyanamide, Chemistry, Thiourea, Oxazolidine, Reactivity (psychology), Urea, Derivative (finance), Medicinal chemistry

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Reactivity of 3,3′‐methylenebis(5‐phenyl)oxazolidine with urea, thiourea and cyanamide. An alternative mechanism for the α‐ureidoalkylation of 2‐amino‐l‐phenylethanol — Research Paper | ScholarLens