An Effective One-Pot Synthesis of 5-Substituted Tetronic Acids.

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چکیده

منابع مشابه

An effective one-pot synthesis of 5-substituted tetronic acids.

An expeditious one-pot synthesis of 5-substituted tetronic acids from aldehydes and terminal conjugated alkyne as starting materials is described. The entire process embodies two consecutive chemical events: a catalytic domino reaction to build the 1,3-dioxolane scaffolds 5 and a two-step acid-catalyzed trans-acetalization-lactonization reaction to furnish the tetronic acid derivatives 6.

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Facile one-pot synthesis of 5-substituted hydantoins.

5-Substituted and 5,5-disubstituted hydantoins are synthesised from the corresponding aldehydes or ketones, using a one-pot, gallium(III) triflate-catalysed procedure that is compatible with a range of substrates and solvents.

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SbCl3 as an Efficient Catalyst for the One-pot Synthesis of Highly Substituted Piperidines

Highly substituted piperidines were synthesized via the condensation of aromatic aldehydes and aromatic amines with β-ketoesters in the presence of antimony(III) chloride at ambient condition. This reaction has any advantages such as easy work-up, clean procedure, and good yields.

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Isothiourea-mediated one-pot synthesis of trifluoromethyl substituted 2-pyrones.

A one-pot isothiourea-mediated Michael addition/lactonization/thiol elimination cascade sequence for the formation of 4,6-disubstituted and 3,4,6-trisubstituted 2-pyrones from (phenylthio)acetic acids and α,β-unsaturated trifluoromethyl ketones is described. The synthesis of a COX-2 inhibitor and the wide-ranging derivatization of the 2-pyrone moiety to trifluoromethyl substituted aromatics and...

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Lewis acid-catalysed one pot synthesis of substituted xanthenes.

A direct synthesis of substituted xanthenes from salicylaldehydes and cyclohexenones or tetralones has been developed. The reaction is catalysed by Lewis acids like scandium triflate and furnishes substituted xanthenes in good to excellent yields using either microwave or thermal heating. Microwave heating results in significantly shortened reaction times of 30 min and generally higher yields.

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ژورنال

عنوان ژورنال: ChemInform

سال: 2003

ISSN: 0931-7597,1522-2667

DOI: 10.1002/chin.200334089