SavedAdd your journal

Journals / Turkish Journal of Chemistry / 2014 / Cilt: 38 - Sayı: 1

Self-condensation reactions of acyl phosphonates: synthesis of tertiary O -protected α-hydroxyphosphonates

Serkan EYMUR
Ayhan Sıtkı DEMİR
Mehmet GÖLLÜ
Pages
164–171
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O -protected α -hydroxy phosphonates in moderate yield.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O -protected α -hydroxy phosphonates in moderate yield.
📊
Key Findings & Data:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O -protected α -hydroxy phosphonates in moderate yield.
💡
Conclusion & Impact:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O -protected α -hydroxy phosphonates in moderate yield.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O -protected α -hydroxy phosphonates in moderate yield.

🔖

Cite This Article

EYMUR, S., DEMİR, A. S., GÖLLÜ, M. (2022). Self-condensation reactions of acyl phosphonates: synthesis of tertiary O -protected α-hydroxyphosphonates. Turkish Journal of Chemistry, Cilt: 38 - Sayı: 1, 164–171. https://ajindex.com/articles/595094

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (4)

  1. Dellaria, J. F., Jr.; Maki, R. G.; Stein, H. H.; Cohen, J.; Whittern, D.; Marsh, K.; Hoffman, D. J.; Plattner, J. J.; Perun, T. J. J. Med. Chem. 1990, 33, 534–542. Tao, M.; Bihovsky, R.; Wells, G. J.; Mallamo, J. P. J. Med. Chem. 1998, 41, 3912–3916. Stowasser, B.; Budt, K. H.; Jian-Qi, L.; Peyman, A.; Ruppert, D. Tetrahedron Lett. 1992, 33, 6625–6628. Pompliano, D. L.; Rands, E.; Schaber, M. D.; Mosser, S. D.; Anthony, N. J.; Gibbs, J. B. Biochemistry 1992, 31, 3800–3807. Hohl, R. J.; Lewis, K. A.; Cermak, D. M.; Wiemer, D. F. Lipids 1998, 33, 39–46. Sikorski, J. A.; Miller, M. J.; Braccolino, D. S.; Cleary, D. G.; Corey, S. D.; Font, J. L.; Gruys, K. J.; Han, C. Y.; Lin, K. C.; Pansegrau, P. D.; et al. Phosphorus Sulfur Silicon Relat. Elem. 1993, 76, 115–117. Snoeck, R.; Holy, A.; Dewolf-Peeters, C.; Van Den Oord, J.; De Clercq, E.; Andrei, G. Antimicrob. Agents Chemother. 2002, 46, 3356–3361. Peters, M. L.; Leonard, M.; Licata, A. A. Clev. Clin. J. Med. 2001, 68, 945–951. Leder, B. Z.; Kronenberg, H. M. Gastroenterology 2000, 119, 866–869. Huber, J. W.; Gilmore, W. F.; Robertson, L. W.; J. Med. Chem. 1975, 18, 106–108. Atherton, F. R.; Hall, M. J.; Hassall, C. H.; Holmes, S.W.; Lambert, R.W.; Lloyd, J.; Ringrose, P. S. Antimicrob. Agents Chemother. 1980, 18, 897–905. Kolodiazhnyi, O. I. Tetrahedron: Asymmetry 1998, 9, 1279–13332. Kolodiazhnyi, O. I. Advances in Asymmetric Synthesis Vol. 3, JAI Press: London, 1998, 273. Kolodiazhnyi, O. I. Russian Chemical Reviews 2006, 75, 227–253. Engel, R. Synthesis of Carbon–Phosphorus Bonds, CRC Press:
  2. Boca Raton, FL, 1987.
  3. Yokomatsu, T.; Yamagishi, T.; Shibuya, S. J. Chem. Soc., Perkin Trans. 1 1997, 1527–1533. Wroblewski, A. E.; Balcerzak, K. B. Tetrahedron: Asymmetry 2001, 12, 427–431. Yokomatsu, T.; Yamagishi, T.; Shibuya, S. Tetrahedron: Asymmetry 1993, 4, 1401–1404. Rowe, B. J.; Spilling, C. D. Tetrahedron: Asymmetry 2001, 12, 1701–1708. Arai, T.; Bougauchi, M.; Sasai, H.; Shibasaki, M. J. Org. Chem. 1996, 61, 2926–2927. Gajda, T. Tetrahedron: Asymmetry 1994, 5, 1965–1972.
  4. Nesterov, V. V.; Kolodiazhnyi, O. I. Zh. Obshch. Khim. 2005, 75, 1225–1229. Meier, C.; Laux, W. H. G. Tetrahedron: Asymmetry 1996, 7, 89–94. Pogatchnik, D. M.; Wiemer, D. F. Tetrahedron Lett. 1997, 38, 3495–3498. Yokomatsu, T.; Yamagishi, T.; Suemune, K.; Yoshida, Y.; Shibuya, S. Tetrahedron 1998, 54, 767–780. Wiemer, D. F.; Kim, D. Y. Tetrahedron Lett. 2003, 44, 2803–2805. Samanta, S.; Zhao, C.-G. J. Am. Chem. Soc. 2006, 128, 7442–7443. Per