Stereoselective multicomponent synthesis of [3-(5-substituted 2-methoxyphenyl)-5-aryl-2-phenyltetrahydro-4-isoxazolyl](2-thienyl)methanones via 1,3-dipolar cycloaddition

Stereoselective multicomponent synthesis of [3-(5-substituted 2-methoxyphenyl)-5-aryl-2-phenyltetrahydro-4-isoxazolyl](2-thienyl)methanones via 1,3-dipolar cycloaddition

Three‐component stereoselective synthesis of a set of new tetra substituted isoxazolidines from 5‐substi‐tuted 2‐methoxybenzaldehydes, N‐phenylhydroxylamine and 1‐(2‐thienyl)‐3‐arylprop‐2‐en‐1‐ones has been achieved. The effect of microwave irradiation on the reaction under solvent‐free conditions h...

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Veröffentlicht in:Journal of heterocyclic chemistry 2005-05, Vol.42 (4), p.515-518
Hauptverfasser: Sridharan, V., Muthusubramanian, S., Saravanakumar, S. Pon
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container_title Journal of heterocyclic chemistry
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creator Sridharan, V.
Muthusubramanian, S.
Saravanakumar, S. Pon
description Three‐component stereoselective synthesis of a set of new tetra substituted isoxazolidines from 5‐substi‐tuted 2‐methoxybenzaldehydes, N‐phenylhydroxylamine and 1‐(2‐thienyl)‐3‐arylprop‐2‐en‐1‐ones has been achieved. The effect of microwave irradiation on the reaction under solvent‐free conditions has also been investigated. The stereochemistry of the final products has been confirmed by NMR and single crystal X‐ray analysis.
doi_str_mv 10.1002/jhet.5570420407
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title Stereoselective multicomponent synthesis of [3-(5-substituted 2-methoxyphenyl)-5-aryl-2-phenyltetrahydro-4-isoxazolyl](2-thienyl)methanones via 1,3-dipolar cycloaddition
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