1996
DOI: 10.1002/chin.199643092
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ChemInform Abstract: Synthesis and Studies of Azolyl Derivatives of 1,3,5‐Triarylpyrazole.

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“…First, this transformation looks like a widely used Robinson-Gabriel oxazole synthesiscyclodehydration of N-acylaminoketones [28][29][30][31][32][33][34][35][36][37], where furan moiety can act as a source of carbonyl group. However, unlike the said method required such as acidic dehydrating agents as acetic anhydride, P 2 O 5 , PPA, triflic anhydride, this transformation proceeds under basic conditions.…”
Section: Resultsmentioning
confidence: 99%
“…First, this transformation looks like a widely used Robinson-Gabriel oxazole synthesiscyclodehydration of N-acylaminoketones [28][29][30][31][32][33][34][35][36][37], where furan moiety can act as a source of carbonyl group. However, unlike the said method required such as acidic dehydrating agents as acetic anhydride, P 2 O 5 , PPA, triflic anhydride, this transformation proceeds under basic conditions.…”
Section: Resultsmentioning
confidence: 99%