Abstract
Thermal condensation of acetals with different thiophosphoramides at 120-160 °C resulted in the formation of the corresponding N-thiophosphoryl imines in good to excellent yield (80-98%) with high purity ( > 95%, determined by 1H NMR and elemental analyses).
Keywords: N-Thiophosphoryl imine, thermal condensation, thiophosphoramide, acetal
Letters in Organic Chemistry
Title: A Convenient and Practical Method for the Synthesis of Aromatic Nthiophosphoryl Imines
Volume: 3 Issue: 8
Author(s): Xinyuan Xu, Chungui Wang, Zhenghong Zhou, Zebing Zeng, Xinpeng Ma, Guofeng Zhao and Chuchi Tang
Affiliation:
Keywords: N-Thiophosphoryl imine, thermal condensation, thiophosphoramide, acetal
Abstract: Thermal condensation of acetals with different thiophosphoramides at 120-160 °C resulted in the formation of the corresponding N-thiophosphoryl imines in good to excellent yield (80-98%) with high purity ( > 95%, determined by 1H NMR and elemental analyses).
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Cite this article as:
Xu Xinyuan, Wang Chungui, Zhou Zhenghong, Zeng Zebing, Ma Xinpeng, Zhao Guofeng and Tang Chuchi, A Convenient and Practical Method for the Synthesis of Aromatic Nthiophosphoryl Imines, Letters in Organic Chemistry 2006; 3 (8) . https://dx.doi.org/10.2174/157017806778559446
DOI https://dx.doi.org/10.2174/157017806778559446 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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