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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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Microwave assisted cycloadditions to [60]fullerene

TL;DR: Under microwave irradiation C 60 undergoes Diels-Alder and 1,3-dipolar cycloadditions within the scale of minutes to afford the respective cycloadducts in similar or increased yields related to the described methods as mentioned in this paper.
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Molten salt ionic liquid-assisted synthesis of nano-structured poly(amide imide)s based on 4,4′-methylenebis(3-chloro-2,6-diethyl trimellit imidobenzene) via microwave process as an environmentally friendly methodology

TL;DR: In this article, a series of self-extinguishing polymers were obtained by direct polycondensation of the synthesized diimide diacid and various commercial diamines using tetra-n-butylammonium bromide and triphenyl phosphite as a condensing agent under microwave irradiation.
Journal ArticleDOI

Microwaves in Chemistry

TL;DR: In this paper, the current outlook for microwaves in chemistry is considered, starting with the theoretical framework for our understanding of microwaves interactions and the causes of results observed, and then survey major application areas including in synthesis and emerging areas in catalysis, energy, and environmental applications.
Journal ArticleDOI

Microwave synthesis of sulfanilic acid

TL;DR: In this paper, the synthesis of sulfanilic acid was modified as the solvent free and microwave assisted experiment under semimicroscale conditions, which is very convenient for the organic chemistry courses in the university or the high school teaching.
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’.
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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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