“…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
Preparation of many kinds of N-, O-, and S-heterocycles from aryl/alkyl alkynyl aldehydes were investigated in recent years. In this review, the synthesis of bioactive heterocycles using by substituted alkynyl aldehydes is highlighted.
“…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
Preparation of many kinds of N-, O-, and S-heterocycles from aryl/alkyl alkynyl aldehydes were investigated in recent years. In this review, the synthesis of bioactive heterocycles using by substituted alkynyl aldehydes is highlighted.
1,3‐Dipolar cycloaddition of in situ generated nitrile oxides with α,β‐acetylenic aldehydes allows the isolation of the expected isoxazoles as single regioisomers.
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