We thank Dr. W: Ppeiderer, Stutrgarf, for synthetic xanthopterin and natural erythropterin, as well as for his suggestions on preparations.
Reaction of thio and seleno phosphoric acid derivatives with O-thioacylated hydroxylamine
✍ Scribed by Grzegorz Cholewinski; Dariusz Witt; Radosław Majewski; Tadeusz Ossowski; Janusz Rachon
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 195 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20368
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The reactivity of thio and seleno analogs of phosphoric acid 1b–f with O‐thioacylhydroxylamine 2 was examined. The experimental evidence for the proposed mechanism involving an N—O bond cleavage and a single electron transfer process (SET) from phosphate anions was collected. The influence of phosphoric acids 1 structure and their oxidation potentials on the course of the reaction and products 3, 4, 6, 7 distribution was presented. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:767–773, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20368
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