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

Research output: Contribution to journalArticle

7 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)1089-1091
Number of pages3
JournalJournal of Heterocyclic Chemistry
Volume31
Issue number4
DOIs
Publication statusPublished - 1994

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Cyanamide
Thiourea
Urea
Derivatives
oxazolidine

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

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. / Pevarello, Paolo; Pinciroli, Vittorio; Varasi, Mario.

In: Journal of Heterocyclic Chemistry, Vol. 31, No. 4, 1994, p. 1089-1091.

Research output: Contribution to journalArticle

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AU - Varasi, Mario

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