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Journal ArticleDOI

Photochemical preparation and rearrangement of some symmetrical methoxypyridyl phenyl glycols (pinacols)

Ellis V. Brown, +1 more
- 01 Dec 1971 - 
- Vol. 8, Iss: 6, pp 967-973
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TLDR
In this paper, 6-methoxy-3-pyridyl phenyl ketone and 3-, 4-, 5- and 6methoxyl-2-polymorphic phenyl isomers were subjected to ultraviolet radiation.
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 1971-12-01. It has received 8 citations till now. The article focuses on the topics: Phenyl group & Isopropyl alcohol.

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Patent

Potassium channel inhibitors

TL;DR: In this article, the present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like, and is related to our present invention.
Journal ArticleDOI

Asymmetrische Synthese bei Photo‐, Elektro‐ und Alkalimetall‐Pinakolisierungen von Benzaldehyd und Phenonen im chiralen Medium DDB

TL;DR: The use and limits of these asymmetric syntheses for the facile preparation of optically active samples, for meso/d,l-assignments, and for mechanistic investigations is briefly discussed in this article.
Journal ArticleDOI

Reductive reactions of substituted pyridines by aqueous titanium trichloride

TL;DR: Aqueous titanium trichloride reductively removes cyano and halo groups from the correspondingly substituted pyridines by a two electron-transfer process and promotes reduction of pyridsyl-ketones and aldehydes to glycols under very simple experimental conditions as discussed by the authors.
Journal ArticleDOI

A convenient synthesis of substituted pyridylgycols promoted by aqueous titanium trichloride

TL;DR: In this paper, the authors proposed a one-pot method to obtain subatituted pyridylglycols in very good yields using a radical mechanism in which the Ti(III) species plays the fundamental role.
Journal ArticleDOI

Late-stage synthesis and application of photoreactive probes derived from direct benzoylation of heteroaromatic C–H bonds

TL;DR: A series of aryl glyoxylic acid reagents featuring pendant alkyne or azide clickable handles have been developed for application in the radical-mediated appendage of benzoyl fragments onto simple heteroaromatic fragments, as well as more complex drug-like compounds.
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