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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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Book ChapterDOI

Recovery of Bioactive Components from Food Processing Waste

TL;DR: In this article, the authors give a brief idea about different extraction techniques which are widely used for extraction of bioactives from food processing waste and describe briefly on recent studies in relation to recovery of bioactive compounds from food waste.
Book ChapterDOI

Reaktoren für spezielle technisch-chemische Prozesse: Mikrowellenreaktoren

TL;DR: In this paper, a Kapitel beschreibt nach einem kurzen historischen Abriss die Technologie and die Vorteile moderner Mikrowellenreaktoren fur die chemische Synthese.
Book ChapterDOI

Microwave-assisted synthesis of quantum dots

TL;DR: In this article , a complete overview has been given on the potential and achievements in the arena of semiconducting and carbon QDs prepared by microwave (MW)-assisted synthesis process only, which has several advantages, including less reaction time, uniform circulation of energy inside the reaction container, environmentally benign, energy conservation, highly reproducible, and exceptional control over experimental limits.
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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