1983
DOI: 10.1055/s-1983-30535
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A New Synthesis of Oxazolo[5,4-d]pyrimid-7-ones

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1984
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Cited by 16 publications
(8 citation statements)
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“…Annulation of pyrimidine rings to 4-carboxy-5-aminooxazoles using a variety of one-carbon synthons. [42] Scheme 32. Ring closure to the desired oxazolopyrimidinones 187 was effectuated by a catalytic amount of sodium ethoxide in good overall yields.…”
Section: Starting From Various Other 245-trisubstituted Oxazolesmentioning
confidence: 99%
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“…Annulation of pyrimidine rings to 4-carboxy-5-aminooxazoles using a variety of one-carbon synthons. [42] Scheme 32. Ring closure to the desired oxazolopyrimidinones 187 was effectuated by a catalytic amount of sodium ethoxide in good overall yields.…”
Section: Starting From Various Other 245-trisubstituted Oxazolesmentioning
confidence: 99%
“…Ring closure to the desired oxazolopyrimidinones 187 was effectuated by a catalytic amount of sodium ethoxide in good overall yields. [42] Unfortunately, the synthesis and characterization of these compounds was not described in detail.…”
Section: Starting From Various Other 245-trisubstituted Oxazolesmentioning
confidence: 99%
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“…This route has some precedence in the literature, (Patil et al, 1971;Turchi et al, 1983;Sekeya et al, 1990) but no cases have been reported in which 2-amino-substituted heterocycles (such as 1) were formed. Our efforts have currently focused on intermediate 4-carboxy-5-ethoxyoxazoles.…”
Section: X)mentioning
confidence: 99%