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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 46, 2016 - Issue 23
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Original Articles

Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including p-methoxybenzyl ethers of alcohols and phenols

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Pages 1893-1901 | Received 24 May 2016, Published online: 03 Sep 2016

References

  • Constable, D. J. C.; Dunn, P. J.; Hayler, J. D.; Humphrey, G. R.; Leazer, J. L.; Linderman, R. J.; Lorenz, K.; Manley, J.; Pearlman, B. A.; Wells, A.; Zaksh, A.; Zhang, T. Y. Green Chem. 2007, 9, 411–420.
  • (a) Forrester, J.; Jones, R. V. H.; Newton, L.; Preston, P. N. Tetrahedron. 2001, 57, 2871–2884; (b) Meyers, A. I.; Ritter, J. J. J. Org. Chem. 1958, 23, 1918–1922; (c) Yasuda, M.; Saito, T.; Ueba, M.; Baba, A. Angew. Chem. Int. Ed. 2004, 43, 1414–1416; (d) Motokura, K.; Nakagiri, N.; Mizugaki, T.; Ebitani, K.; Kaneda, K. J. Org. Chem. 2007, 72, 6006–6015.
  • (a) Zhao, X.; Zhuang, W.; Fang, D.; Xue, X.; Zhou, J. Synlett 2009, 779–782; (b) Castro, B. R. Org. React. 1983, 29, 1–126.
  • (a) Mitsunobu, O.; Yamada, Y. Bull. Chem. Soc. Jap. 1967, 40, 2380–2382; (b) Mitsunobu, O. Synthesis 1981, 1, 1–28; (c) Swamy, K. C.; Kumar, N. N.; Balaraman, E.; Kumar, K. V. Chem. Rev. 2009, 109, 2551–2651.
  • (a) Feuer, H.; Hoz, J. The chemistry of the ether linkage; in S. Patai (Ed.); Interscience: London, 1967; 457–472; (b) Larock, R. C. Comprehensive Organic Transformations, 2nd ed.; Wiley/Interscience: New York, 1999; pp. 897–910.
  • (a) Kim, S.; Chung, K. N.; Yang, S. J. Org. Chem. 1987, 52, 3917–3919; (b) Salehi, P.; Iranpoor, N.; Behbahani, F. K. Tetrahedron 1998, 54, 943–948; (c) Jiang, R.; Shen, Y.; Zhang, Y.; Xu, X.; Shao, J.; Ji, S. Chin. J. Chem. 2011, 29, 1887–1893; (d) Diaz, D. D.; Martin, V. S. Tetrahedron Lett. 2000, 41, 9993–9996; (e) Shibata, T.; Fujiwara, R.; Ueno, Y. Synlett 2005, 1, 152–154; (f) Boyer, B.; Keramane, E. M.; Roque, J. P.; Pavia, A. A. Tetrahedron Lett. 2000, 41, 2891–2894; (g) Bikard, Y.; Weibel, J.; Sirlin, C.; Dupuis, L.; Loefflerc, J.; Palea, P. Tetrahedron Lett. 2007, 48, 8895–8899; (h) Cuenca, A. B.; Mancha, G.; Asensio, G.; Medio-Simon, M. Chem. Eur. J. 2008, 14, 1518–1523 (i) Prades, A.; Corbe, R.; Poyatos, M.; Peris, E. Chem. Eur. J. 2008, 14, 11474–11479; (j) Yu, J.; Wang, H.; Zou, K.; Zhang, J.; Gao, X.; Zhang, D.; Li, Z. Tetrahedron 2013, 69, 310–315; (k) Kim, J.; Lee, D.-H.; Kalutharage, N.; Yi, C. S. ACS Catal. 2014, 4, 3881–3885.
  • (a) Firouzabadi, H.; Iranpoor, N.; Jafari, A. A. J.Mol. Catal. A: Chem. 2005, 227, 97–100; (b) Corma, A.; Renz, M. Angew. Chem., Int. Ed. 2007, 46, 298–300 (c) Rao, K. T. V.; Rao, P. S. N.; Sai Prasad, P. S.; Lingaiah, N. Catal. Commun. 2009, 10, 1394–1397; (d) Mitsudome, T.; Matsuno, T.; Sueoka, S.; Mizugaki, T.; Jitsukawaa, K.; Kaneda, I. Green Chem. 2012, 14, 610–613.
  • (a) Green, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis; John Wiley & Sons: New York, 1999; pp. 23–201; (b) Hinklin, R. J.; Kiessling, L. L. Org. Lett. 2002, 4, 1131–1133.
  • (a) McCloskey, C. M. Adv. Carbohydr. Chem. 1957, 12, 137; (b) Kasprzycka, A.; Ptaszek-Budniok, A.; Szeja, W. Synth. Commun. 2014, 44, 2276–2284; (c) Czernecki, S.; Georgoulis, C.; Provelenghiou, C. Tetrahedron Lett. 1976, 17, 3535–3536.
  • Brewer, S. E.; Vickery, T. P.; Bachert, D. C.; Brands, K. M. J.; Emerson, K. M.; Goodyear, A.; Kumke, K. J.; Lam, T.; Scott, J. P. Org. Process Res. Dev. 2005, 9, 1009–1012.
  • (a) Chaudhari, P. S.; Salim, S. D.; Sawant, R. V.; Akamanchi, K. G. Green Chem. 2010, 12, 1707–1709; (b) Katkar, K. V.; Chaudhari, P. S.; Akamanchi, K. G. Green Chem. 2011, 13, 835–838; (c) Salim, S. D.; Akamanchi, K. G. Catal. Comm. 2011, 12, 1153–1156; (d) Salim, S. D.; Pathare, S. P.; Akamanchi, K. G. Catal. Commun. 2011, 12, 78–81; (e) Pathare, S. P.; Akamanchi, K. G. Tetrahedron Lett. 2012, 53, 871–875; (f) Pathare, S. P.; Chaudhari, P. S.; Akamanchi, K. G. Appl. Catal. A: Gen. 2012, 425–426, 125–129; (g) Pathare, S. P.; Sawant, R. V.; Akamanchi, K. G. Tetrahedron Lett. 2012, 53, 3259–3263; (h) Pathare, S. P.; Jain, A. H.; Akamanchi, K. G. RSC Adv. 2013, 3, 7697; (i) Veer, S. D.; Pathare, S. P.; Akamanchi, K. G. Arkivoc 2016, 4, 59–66; (j) Pathare, S. P.; Akamanchi, K. G. Appl. Catal. A: Gen. 2013, 452, 29–33.

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