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Bioscience, Biotechnology, and Biochemistry Volume 57, 1993 - Issue 9
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Synthetic Reactions in PEG: PEG-Assisted Synthesis of 2-Cyano-6-methoxybenzothiazole, A Key Intermediate For The Synthesis of Firefly Luciferin

Nobutaka SuzukiShimonoseki University of Fisheries, Yoshimi, Shimonoseki759–65, Japan
,
Tateo NomotoDepartment of Chemistry, Faculty of Education, Mie University, Tsu 514, Japan
,
Yoshiaki ToyaAichi University of Education, Kariya, Aichi448, Japan
,
Norio KanamoriTokushima University School of Dentistry, Tokushima770, Japan
,
Binkoh YodaKoriyama Women’s University, Koriyama, Fukushima963, Japan
&
Akio SaekiTohoku Institute of Technology, Yagiyama, Taihaku, Sendai982, Japan
Pages 1561-1562 | Received 14 Dec 1992, Published online: 12 Jun 2014

References

  • Preceding report in this series: N. Suzuki, T. Azuma, K. Watanabe, T. Nomoto, Y. lzawa, and H. Tomioka, J. Chem. Soc., Perkin Trans. 1, 1987, 1951–1953; N. Suzuki, T. Azuma, T. Nomoto, and Y. Izawa, Chem. Ind. (London), 1985, 698–699.
  • N. Suzuki, K. Shimazu, T. Ito, and Y. Izawa, J. Chem. Soc., Chem. Commun., 1980, 1253–1255; N. Suzuki, K. Shimazu, T. Ito, and Y. Izawa, in Polymer Science and Technology, Vol. 24, “Crown Ethers and Phase Transfer Catalysis in Polymer Science,” ed. by L. J. Mathias and C. E. Carraher, 1984, Plenum Press, New York, pp. 385–396.
  • N. Suzuki, Y. Ayaguchi, and Y. Izawa, Bull. Chem. Soc. Jpn., 55, 3349–3350 (1982).
  • N. Suzuki, Y. Kaneko, T. Nomoto, and Y. lzawa, J. Chem. Soc., Chem. Commun., 1984, 1523–1524; N. Suzuki, T. Azuma, Y. Kaneko, T. Nomoto, Y. Izawa, and H. Tomioka, J. Chem. Soc., Perkin Trans. 1, 1987, 645–647.
  • E. Santaniello, A. Manzocchi, and P. Sozzani, Tetrahedron Lett., 1979, 4581–4582.
  • K. Sukata, J. Synth. Org. Chem. Jpn., 39, 443–444 (1981).
  • N. Suzuki, Y. Ayaguchi, and Y. lzawa, Chem. Ind. (London), 1983, 166; N. Suzuki, Y. Ayaguchi, T. Tsukanaka, and Y. Izawa, Bull. Chem. Soc. Jpn., 56, 353–354 (1983).
  • N. Suzuki, T. Tsukanaka, T. Nomoto, Y. Ayaguchi, and Y. Izawa, J. Chem. Soc., Chem. Commun., 1983, 515–516; N. Suzuki, Y. Kaneko, T. Tsukanaka, T. Nomoto, Y. Ayaguchi, and Y. Izawa, Tetrahedron, 41, 2387–2392 (1985).
  • E. Santaniello, P. Ferraboschi, and P. Sozzani, J. Org. Chem., 46, 4584–4585 (1981).
  • E. Santaniello, A. Fiecchi, A. Manzocchi, and P. Ferraboschi, J. Org. Chem., 48, 3074–3077 (1983).
  • E. H. White, F. McCapra, and G. F. Field, J. Am. Chem. Soc., 85, 337–343 (1963).
  • S. Seto, K. Ogura, and Y. Nishiyama, Bull. Chem. Soc. Jpn., 36, 331–333 (1963).
  • E. H. White, H. Woerther, G. F. Field, and W. D. McElroy, J. Org. . Chem., 30, 2344–2348 (1965).
  • L. J. Bowie, Methods Enzyinol., 57, 15–28 (1978).
  • Y. Toya, M. Takagi, H. Nakata, N. Suzuki, M. Isobe, and T. Ooto, Bull. Chem. Soc. Jpn., 65, 392–395 (1992).
  • M. P. Doyle, B. Siegfried, J. F. Dellaria, J. Org. Chem., 42, 2426–2431 (1977).
  • S. R. Sandler and W. Karo, in “Organic Functional Group Preparations,” Vol. 1, Academic Press, New York, 1983, p. 560.
  • “The Aldrich Library of Infrared Spectra,” Vol. 2, ed. by C. J. . Pouchert, 2nd Ed., 1113D, Aldrich chem., Milwaukee, WI, 1975.
  • “The Aldrich Library of NMR Spectra,” Vol. 8, ed. by C. J. Pouchert, 98B, Aldrich chem. Co., Milwaukee, WI, 1974.

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