The Reaction of Perezone and Isoperezone with Hydroxylamine: A Surprisingly Facile Method for Introducing an NH2Group into the Quinone Functionality-Reference-Cited by-同舟云学术

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The Reaction of Perezone and Isoperezone with Hydroxylamine: A Surprisingly Facile Method for Introducing an NH2Group into the Quinone Functionality

Published:1995-04 Issue:2 Volume:6 Page:103-109
ISSN:1057-5634
Container-title:Natural Product Letters
language:en
Short-container-title:Natural Product Letters

Author:

Enríquez Raúl G.,Ortiz Benjamín,Alducin Enrique,Walls Fernando,Gnecco Dino,Yu Margaret,Reynolds William F.

Publisher

Informa UK Limited

Subject

Molecular Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/10575639508044097

Reference29 articles.

1. de la Loza, L. Río. 1852. Dissertation presented to the Academy of Medicine. October 301852, Méx.

2. A correction of the structure of perezone

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Perezone and its phenyl glycine derivative induce cytotoxicity via caspases on human glial cancer cells;Natural Product Research;2023-06-21

2. Resumen Histórico sobre la perezona, 1852-2022;TECNOCIENCIA Chihuahua;2022-10-19

3. A Timeline of Perezone, the First Isolated Secondary Metabolite in the New World, Covering the Period from 1852 to 2020;Progress in the Chemistry of Organic Natural Products;2021

4. Characterization and comparison of perezone with some analogues. Experimental and theoretical study;Journal of Molecular Structure;2015-10

5. Lumiquinone A, an α-Aminomalonate-Derived Aminobenzoquinone from Photorhabdus luminescens;Journal of Natural Products;2015-05-19

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