2016
DOI: 10.1016/j.tetlet.2016.01.019
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Highly regioselective dipolar cycloadditions of nitrile oxides with α,β-acetylenic aldehydes

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Cited by 15 publications
(1 citation statement)
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“…Both alkynyl aldehydes 1a and oximes 58a bearing aryl, heteroaryl and alkyl groups were compatible in this transformation ( Scheme 80 ). 94 Preparation and cytotoxic evaluation of isoxazoles 59b and pyrazoles 59d were performed by Praveen et al ( Scheme 81 ). 95 In this regard, they investigated the capability of AuCl 3 in the cycloisomerization of α,β-acetylenic oximes 59a and α,β-acetylenic hydrazones 59c.…”
Section: Synthesis Of On-heterocyclic Compoundsmentioning
confidence: 99%
“…Both alkynyl aldehydes 1a and oximes 58a bearing aryl, heteroaryl and alkyl groups were compatible in this transformation ( Scheme 80 ). 94 Preparation and cytotoxic evaluation of isoxazoles 59b and pyrazoles 59d were performed by Praveen et al ( Scheme 81 ). 95 In this regard, they investigated the capability of AuCl 3 in the cycloisomerization of α,β-acetylenic oximes 59a and α,β-acetylenic hydrazones 59c.…”
Section: Synthesis Of On-heterocyclic Compoundsmentioning
confidence: 99%