Lewis Acid-Promoted Disproportionation Reaction of Aromatic Vinyl Ethers and Acetals and Its Application to the Synthesis of Paracotoin

Bulletin of the Chemical Society of Japan

Volumn 71, Issue 9, 1998, Pages 2181-2185

  Gong, Young Dae ^a   Tanaka, Hiroko ^a   Iwasawa, Nobuharu ^a   Narasaka, Koichi ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000627317     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.71.2181     Document Type: Article

References (23)

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4. For examples, see: a) E. Kitazawa, T. Imamura, K. Saigo, and T. Mukaiyama, Chem. Lett., 1975, 569; b) U. Brüggen, R. Lammers, and H. Mayr, J. Org. Chem., 53, 2920 (1988).
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6. 2). Their reactions are limited to cyclic ketones, in particular, cyclopentenones. See the following references; further references are cited therein. a) H. Suemune, O. Yoshida, J. Uchida, Y. Nomura, M. Tanaka, and K. Sakai, Tetrahedron Lett., 36, 7259 (1995); b) S. Nagumo, A. Matsukuma, H. Suemune, and K. Sakai, Tetrahedron, 49, 10501 (1993); T. Yamamoto, T. Eki, S. Nagumo, H. Suemune, and K. Sakai, Tetrahedron, 48, 4517 (1992).
7. 2). Their reactions are limited to cyclic ketones, in particular, cyclopentenones. See the following references; further references are cited therein. a) H. Suemune, O. Yoshida, J. Uchida, Y. Nomura, M. Tanaka, and K. Sakai, Tetrahedron Lett., 36, 7259 (1995); b) S. Nagumo, A. Matsukuma, H. Suemune, and K. Sakai, Tetrahedron, 49, 10501 (1993); T. Yamamoto, T. Eki, S. Nagumo, H. Suemune, and K. Sakai, Tetrahedron, 48, 4517 (1992).
8. 2). Their reactions are limited to cyclic ketones, in particular, cyclopentenones. See the following references; further references are cited therein. a) H. Suemune, O. Yoshida, J. Uchida, Y. Nomura, M. Tanaka, and K. Sakai, Tetrahedron Lett., 36, 7259 (1995); b) S. Nagumo, A. Matsukuma, H. Suemune, and K. Sakai, Tetrahedron, 49, 10501 (1993); T. Yamamoto, T. Eki, S. Nagumo, H. Suemune, and K. Sakai, Tetrahedron, 48, 4517 (1992).
9. For recent examples of indium mediated reactions, see: a) V. J. Bryan and T. H. Chan, Tetrahedron Lett., 38, 6493 (1997); b) C. J. Li, D. L. Chen, Y. Q. Lu, J. X. Haberman, and J. T. Mague, J. Am. Chem. Soc., 118, 4216 (1996); c) L. A. Paquette and P. C. Lobben, J. Am. Chem. Soc., 118, 1917 (1996); d) S. Araki, H. Ito, and Y. Butugan, J. Org. Chem., 53, 1831 (1988).
10. For recent examples of indium mediated reactions, see: a) V. J. Bryan and T. H. Chan, Tetrahedron Lett., 38, 6493 (1997); b) C. J. Li, D. L. Chen, Y. Q. Lu, J. X. Haberman, and J. T. Mague, J. Am. Chem. Soc., 118, 4216 (1996); c) L. A. Paquette and P. C. Lobben, J. Am. Chem. Soc., 118, 1917 (1996); d) S. Araki, H. Ito, and Y. Butugan, J. Org. Chem., 53, 1831 (1988).
11. For recent examples of indium mediated reactions, see: a) V. J. Bryan and T. H. Chan, Tetrahedron Lett., 38, 6493 (1997); b) C. J. Li, D. L. Chen, Y. Q. Lu, J. X. Haberman, and J. T. Mague, J. Am. Chem. Soc., 118, 4216 (1996); c) L. A. Paquette and P. C. Lobben, J. Am. Chem. Soc., 118, 1917 (1996); d) S. Araki, H. Ito, and Y. Butugan, J. Org. Chem., 53, 1831 (1988).
12. For recent examples of indium mediated reactions, see: a) V. J. Bryan and T. H. Chan, Tetrahedron Lett., 38, 6493 (1997); b) C. J. Li, D. L. Chen, Y. Q. Lu, J. X. Haberman, and J. T. Mague, J. Am. Chem. Soc., 118, 4216 (1996); c) L. A. Paquette and P. C. Lobben, J. Am. Chem. Soc., 118, 1917 (1996); d) S. Araki, H. Ito, and Y. Butugan, J. Org. Chem., 53, 1831 (1988).
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