Preparation of (R)-(-)-2-methoxy-2′-(1H-tetrazol-5-yl)-1,1′-binaphthyl and (1R, 2R)-(+)-1-trimethylsilyl-2-(1H-tetrazol-5-yl)ferrocene: Optically active tetrazoles with axial or planar chirality

Synlett

Volumn , Issue SPEC. ISS., 1997, Pages 495-497

  Hirose, Masaaki ^a   Kawai, Rie ^a   Hayakawa, Yoshihiro ^a  

^a NAGOYA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0005613322     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-6151     Document Type: Article

References (45)

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11. 3) δ 3.85 (s, 3H), 6.90 (d, J = 9.2 Hz, 1H), 7.22-7.40 (m, 3H), 7.48 (d, J = 8.9 Hz, 1H), 7.60 (ddd, J = 2.0, 5.9, and 8.3 Hz, 1H), 7.79 (d, J = 8.6 Hz, 1H), 7.88-8.08 ppm (m, 4H). This compound can be prepred in lower yield by the method reported in Miyano, S.; Okada, S.; Hotta, H.; Takeda, M.; Suzuki, T.; Kabuto, C.; Yasuhara, F. Bull. Chem. Soc. Jpn. 1989, 62, 3886.
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13. 3) δ 3.54 (s, 3H), 7.00-7.21 (m, 5H), 7.31 (d, J = 9.2 Hz, 1H), 7.40 (m, 1H), 7.73 (d, J = 8.3 Hz, 1H), 7.83 (d, J = 8.9 Hz, 1H), 7.90 (d, J = 8.3 Hz, 1H), 7.98 (d, J = 8.6 Hz, 1H), 8.36 (d, J = 8.6 Hz, 1H), 11.4 ppm (brs, 1H).
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17. 3) δ 0.36 (s, 9H), 4.14 (s, 5H), 4.27 (m, 1H), 4.45 (t, J = 2.3 Hz, 1H), 5.15 ppm (m, 1H).
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