Cation Radical-Nucleophile Combination Reactions. Reactions of Nitrogen-Centered Nucleophiles with Cation Radicals Derived from Anthracenes

DOI: 10.1021/ja00018a037

Source and publish data:

Journal of the American Chemical Society p. 6954 - 6958 (1991)

Update date:2022-08-04

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Authors:

Reitstoeen, Bjoern

Parker, Vernon D.

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Article abstract of DOI:10.1021/ja00018a037

Cation radicals derived from anthracene and 9-substituted anthracenes react with pyridine and substituted pyridines to form pyridinium salts. 9-Nitro- and 9-cyano-substituted cation radicals were observed to be about 10² times as reactive as un

Full text of DOI:10.1021/ja00018a037

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Article Doi

Cation Radical-Nucleophile Combination Reactions. Reactions of Nitrogen-Centered Nucleophiles with Cation Radicals Derived from Anthracenes

DOI: 10.1021/ja00018a037

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00018a037

Full text of DOI:10.1021/ja00018a037

Products guided by the article

R&D Labs maybe for 142311-00-0

Relevant to this article

2,6-Disubstituted Aryl Carboxylic Acids, Leaving Groups "Par Excellence" for Benzisothiazolone Inhibitors of Human Leukocyte Elastase

InCl3 catalysed one-pot synthesis of substituted pyrroles and 2-pyrones

Discovery of a novel class of highly potent, selective, ATP-competitive, and orally bioavailable inhibitors of the mammalian target of rapamycin (mTOR)

Azo complexes of osmium(II): Preparation and reactivity of organic azide and hydrazine derivatives

Synthesis, characterization, and antimicrobial activity of benzimidazole-derived chalcones containing 1,3,4-oxadiazole moiety

InCl₃ catalysed one-pot synthesis of substituted pyrroles and 2-pyrones