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Journal ArticleDOI

Application of commercial microwave ovens to organic synthesis.

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TLDR
In this article, commercial microwave ovens have been safely used to dramatically reduce the reaction times (at comparable yield) of Diels-Alder, Claisen, and ene reactions.
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This article is published in Tetrahedron Letters.The article was published on 1986-01-01. It has received 1028 citations till now. The article focuses on the topics: Microwave oven.

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Citations
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Book ChapterDOI

Solvent-free Reactions

TL;DR: A comprehensive review of solvent-free methods for microwave activation can be found in this article with microwave activation as a beneficial alternative to conventional heating under safe and efficient conditions with large enhancements in yields and savings in time.
Journal ArticleDOI

A simple continuous flow microwave reactor

TL;DR: A new simple procedure for microwave-assisted organic synthesis under continuous flow processing has been developed for use in a monomodal microwave synthesizer with direct temperature control using the instrument's in-built IR sensor.
Journal ArticleDOI

Aqueous hydrotrope solution as a safer medium for microwave enhanced hantzsch dihydropyridine ester synthesis

TL;DR: In this article, the first Hautzsch esters were prepared by condensing alkyl β-aminoerotonate, aldehyde and alkyls acetoacetate in aqueous sodium butylmonoglycolsulphate (NaBMGS) as a safe reaction medium in an unmodified domestic microwave oven.
Journal ArticleDOI

Advances in biomass transformation to 5-hydroxymethylfurfural and mechanistic aspects

TL;DR: In this paper, a review of 5-hydroxymethylfurfural (HMF) production from cellulose and lignocelluloses and mechanistic aspects of HMF formation is presented to bridge the gap in understanding the factors responsible for selective conversion and selection of catalyst.
References
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Journal ArticleDOI

The reaction of anthracene with maleic and fumaric acid and their derivatives and with citraconic anhydride and mesaconic acid.

TL;DR: The initial precipitate of long dense needles had become contaminated by a small superficial layer of fluffy crystalline balls, apparently containing the saturated dioltrione (XXIV) and after two further recrystallizations from alcohol melted at 23!-238’.
Journal ArticleDOI

Chlorination of organoboranes: synthesis of (z)-vinyl chlorides

TL;DR: Chloration d'(alcene-1yl dihydroxy) boranes et obtention stereoselective de cis-chloro-1 alcenes as mentioned in this paper.
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