Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Solvent-free Cleavage of tert-Butyl Esters under Microwave Conditions

  • Published : 2009.01.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Green, T. W.; Wuts, P. G. Protective Groups in Organic Synthesis, 4th ed.; John Wiley & Sons: New York, 2007
  2. Kocienski, P. J. Protecting Groups, 3rd ed.; George Thieme Stuttgart: New York, 2004
  3. Bryan, D. B.; Hall, R. F.; Holden, K. G.; Huffman, W. F.; Gleason, J. G. J. Am. Chem. Soc. 1977, 99, 2353 https://doi.org/10.1021/ja00449a063
  4. Strazzolini, P.; Dall'Arche, M. G.; Giumanini, A. G. Tetrahedron Lett. 1998, 39, 9255 https://doi.org/10.1016/S0040-4039(98)02079-6
  5. Strazzolini, P.; Scuccato, M.; Giuanini, A. G. Tetrahedron 2000, 56, 3625 https://doi.org/10.1016/S0040-4020(00)00280-5
  6. Strazzolini, P.; Misuri, N.; Polese, P. Tetrahedron Lett. 2005, 46, 2075 https://doi.org/10.1016/j.tetlet.2005.01.129
  7. Martinez, A. G.; Barcina, J. O.; Veccio, G. H. d.; Hanack, M.; Subramanian, L. R. Tetrahedron Lett. 1991, 32, 5931 https://doi.org/10.1016/S0040-4039(00)79429-9
  8. Wu, Y.-q.; Limburg, D. C.; Wilkinson, D. E.; Vaal, M. J.; Hamilton, G. S. Tetrahedron Lett. 2000, 41, 2847 https://doi.org/10.1016/S0040-4039(00)00300-2
  9. Kaul, R.; Brouillette, Y.; Sajjadi, Z.; Hansford, K. A.; Lubell, W. D. J. Org.Chem. 2004, 69, 6131 https://doi.org/10.1021/jo0491206
  10. Jackson, R. W. Tetrahedron Lett. 2001, 42, 5163 https://doi.org/10.1016/S0040-4039(01)00980-7
  11. Caddick, S. Tetrahedron 1995, 51, 10403 https://doi.org/10.1016/0040-4020(95)00662-R
  12. Loupy, A. Microwave in Organic Synthesis; Wiley-VCH: Weinheim, 2002
  13. Varma, R. S. Pure and Applied Chemistry 2001, 73, 193 https://doi.org/10.1351/pac200173010193
  14. Park, S. H. Bull. Korean Chem. Soc. 2003, 24, 253 https://doi.org/10.1007/s11814-007-5038-8
  15. Park, S. H.; Gwon, H. J.; Lee, H. S.; Park, K. B. Bull. Korean Chem. Soc. 2005, 26, 1701 https://doi.org/10.5012/bkcs.2005.26.11.1701
  16. Jo, E. A.; Ahn, J. A.; Jun, C. H. Bull. Korean Chem. Soc. 2007, 28, 2020 https://doi.org/10.5012/bkcs.2007.28.11.2020
  17. Yadav, J. S.; Reddy, B. V. S.; Shankar, K. S.; Swamy, T.; Premalatha, K. Bull. Korean Chem. Soc. 2008, 29, 1418 https://doi.org/10.5012/bkcs.2008.29.7.1418
  18. Lee, J. C.; Yoo, E. S.; Lee, J. S. Synth. Comm. 2004, 34, 3017 https://doi.org/10.1081/SCC-200026661

Cited by

  1. Heteroaryl Hydroxycarbonylation: An Efficient, Robust, Practically Scalable Approach Using Formyl Acetate as the CO Source vol.42, pp.5, 2012, https://doi.org/10.1080/00397911.2010.528851
  2. Homogeneous and heterogeneous catalytic (dehydrogenative) oxidation of oleochemical 1,2-diols to α-hydroxyketones vol.19, pp.14, 2017, https://doi.org/10.1039/C7GC00867H
  3. ChemInform Abstract: Solvent-Free Cleavage of tert-Butyl Esters under Microwave Conditions. vol.40, pp.27, 2009, https://doi.org/10.1002/chin.200927064
  4. Synthesis of the 1,3,4‐Oxadiazole Core through Thermolysis of Geminal Diazides vol.2016, pp.34, 2009, https://doi.org/10.1002/ejoc.201601119