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Volumn 67, Issue 25, 2002, Pages 8711-8720

Light-induced geometric isomerization of 1,2-diphenylcyclopropanes included within Y zeolites: Role of Cation-guest binding

Author keywords

[No Author keywords available]

Indexed keywords

DERIVATIVES; ISOMERIZATION; PHOTOCHEMICAL REACTIONS; POSITIVE IONS; ZEOLITES;

EID: 0037073877     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026137k     Document Type: Article
Times cited : (28)

References (93)
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    • For reviews on asymmetric induction in organic photochemistry, see: (a) Rau, H. Chem. Rev. 1983, 83, 535. (b) Inoue, Y. Chem. Rev. 1992, 92, 741. (c) Pete, J. P. Adv. Photochem. 1996, 21, 135. (d) Everitt, S. R. L.; Inoue, Y. In Molecular and Supramolecular Photochemistry; Ramamurthy, V., Schanze, K. S., Eds.; Marcel Dekker: New York, 1999; p 71.
    • (1983) Chem. Rev. , vol.83 , pp. 535
    • Rau, H.1
  • 9
    • 0001013736 scopus 로고
    • For reviews on asymmetric induction in organic photochemistry, see: (a) Rau, H. Chem. Rev. 1983, 83, 535. (b) Inoue, Y. Chem. Rev. 1992, 92, 741. (c) Pete, J. P. Adv. Photochem. 1996, 21, 135. (d) Everitt, S. R. L.; Inoue, Y. In Molecular and Supramolecular Photochemistry; Ramamurthy, V., Schanze, K. S., Eds.; Marcel Dekker: New York, 1999; p 71.
    • (1992) Chem. Rev. , vol.92 , pp. 741
    • Inoue, Y.1
  • 10
    • 85050326151 scopus 로고    scopus 로고
    • For reviews on asymmetric induction in organic photochemistry, see: (a) Rau, H. Chem. Rev. 1983, 83, 535. (b) Inoue, Y. Chem. Rev. 1992, 92, 741. (c) Pete, J. P. Adv. Photochem. 1996, 21, 135. (d) Everitt, S. R. L.; Inoue, Y. In Molecular and Supramolecular Photochemistry; Ramamurthy, V., Schanze, K. S., Eds.; Marcel Dekker: New York, 1999; p 71.
    • (1996) Adv. Photochem. , vol.21 , pp. 135
    • Pete, J.P.1
  • 11
    • 0002558540 scopus 로고    scopus 로고
    • Ramamurthy, V., Schanze, K. S., Eds.; Marcel Dekker: New York
    • For reviews on asymmetric induction in organic photochemistry, see: (a) Rau, H. Chem. Rev. 1983, 83, 535. (b) Inoue, Y. Chem. Rev. 1992, 92, 741. (c) Pete, J. P. Adv. Photochem. 1996, 21, 135. (d) Everitt, S. R. L.; Inoue, Y. In Molecular and Supramolecular Photochemistry; Ramamurthy, V., Schanze, K. S., Eds.; Marcel Dekker: New York, 1999; p 71.
    • (1999) Molecular and Supramolecular Photochemistry , pp. 71
    • Everitt, S.R.L.1    Inoue, Y.2
  • 55
    • 0012144187 scopus 로고    scopus 로고
    • Irradiations of pure diastereomers of the trans isomer of α-methylbenzyl amide of 2β,3β-diphenylcyclopropane-1α-carboxylic acid have shown that upon triplet sensitization a common intermediate results that leads to racemization while upon direct excitation leads to an intermediate where the diastereomers do not interconvert. Sivaguru, J.; Shichi, T.; Ramamurthy, V. Org. Lett. 2002, 4, 4221-4224.
    • (2002) Org. Lett. , vol.4 , pp. 4221-4224
    • Sivaguru, J.1    Shichi, T.2    Ramamurthy, V.3
  • 74
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    • Traecy, M. M. J., Marcus, B. K., Bisher, B. E., Higgins J. B., Eds.; Materials Research Society: Warrendale, PA
    • (e) Joy, A.; Corbin, D. R.; Ramamurthy, V. In Proceedings of 12th International Zeolite Conference; Traecy, M. M. J., Marcus, B. K., Bisher, B. E., Higgins, J. B., Eds.; Materials Research Society: Warrendale, PA, 1999; p 2095.
    • (1999) Proceedings of 12th International Zeolite Conference , pp. 2095
    • Joy, A.1    Corbin, D.R.2    Ramamurthy, V.3
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    • note
    • (c) 2β,3β-Diphenylcyclopropane-1α-carboxylic acid was synthesized by using cis-stilbene, and rac-2,3-diphenylcyclopropane-1-carboxylic acid was synthesized using trans· stilbene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.