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Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected alpha-hydroxyphosphonates
Date
2014-01-01
Author
EYMUR, SERKAN
Gollu, Mehmet
Demir, Ayhan Sıtkı
Metadata
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This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
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The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected alpha-hydroxy phosphonates in moderate yield.
Subject Keywords
General Chemistry
URI
https://hdl.handle.net/11511/51020
Journal
TURKISH JOURNAL OF CHEMISTRY
DOI
https://doi.org/10.3906/kim-1306-7
Collections
Department of Chemistry, Article
Citation Formats
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ACM
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BibTeX
S. EYMUR, M. Gollu, and A. S. Demir, “Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected alpha-hydroxyphosphonates,”
TURKISH JOURNAL OF CHEMISTRY
, vol. 38, no. 1, pp. 164–171, 2014, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/51020.
