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Journal ArticleDOI

Synthesis of azirines containing aldehyde functionality and their utilization as synthetic tools for five membered oxazoles and isoxazoles

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TLDR
In this article, a simple and useful procedure for the synthesis of azirines containing aldehyde functionality from open chain bromo/chloro-aldehydes at room temperature is reported.
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 2008-03-01. It has received 32 citations till now. The article focuses on the topics: Lewis acids and bases & Aldehyde.

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Expedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethers

TL;DR: Novel rearrangements of α-oximino ketenes derived from α-diazo oxime ethers provides 2H-azirines bearing quaternary centers and allows for subsequent rearrangement to highly substituted pyrroles in excellent yields.
Journal ArticleDOI

Synthesis of Pyridines by Carbenoid‐Mediated Ring Opening of 2H‐Azirines

TL;DR: In this article, a novel strategy of activation of 2H-aziridines provides a broad range of highly conjugated poly-arylpyridine systems by formal [3 + 3]-cycloaddition.
Journal ArticleDOI

The synthetic and therapeutic expedition of isoxazole and its analogs

TL;DR: This review is an endeavor to highlight the progress in the chemistry and biological activity of isoxazole derivatives which could provide a low-height flying bird’s eye view to the medicinal chemists for the development of clinically viable drugs using this information.
Journal ArticleDOI

[3 + 2] Cycloaddition/Oxidative Aromatization Sequence via Photoredox Catalysis: One-Pot Synthesis of Oxazoles from 2H-Azirines and Aldehydes.

TL;DR: A novel [3 + 2] cycloaddition/oxidative aromatization sequence via visible light-induced photoredox catalysis is disclosed and provides a general synthetic route to 2,4,5-trisubstituted oxazoles from easily accessible 2H-azirines and aldehydes under mild reaction conditions.
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