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Volumn 65, Issue 20, 2000, Pages 6354-6361

New substituent effects of the trimethylsilyl group: Photochemistry of 3-trimethylsilyl-2,5,-cyclohexadienones and preparation of 4-alkylidenecyclopentenones

Author keywords

[No Author keywords available]

Indexed keywords

3 TRIMETHYLSILYL 2,5 CYCLOHEXADIENONE; BENZOIC ACID DERIVATIVE; BICYCLO COMPOUND; CYCLOPENTENONE DERIVATIVE; TRIMETHYLSILYL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034613324     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000209v     Document Type: Article
Times cited : (8)

References (42)
  • 1
    • 0038390916 scopus 로고
    • Cyclohexadienone Photochemistry: Trapping Reactions
    • Horspool, W. M., Song; P.-S., Eds.; CRC Press: London
    • For a review of the intramolecular trapping reactions of 2,5-cyclohexadien-1-ones, see: Schultz, A. G. Cyclohexadienone Photochemistry: Trapping Reactions. In CRC Handbook of Organic Photochemistry; Horspool, W. M., Song; P.-S., Eds.; CRC Press: London, 1995; pp 716-727.
    • (1995) CRC Handbook of Organic Photochemistry , pp. 716-727
    • Schultz, A.G.1
  • 31
    • 84986366757 scopus 로고
    • 4-Alkylidene-2-cyclopenten-1-ones also have been obtained as reaction byproducts; for example, see: (a) Ackroyd, J.; Karpf, M.; Dreiding, A. S. Helv. Chim. Acta 1985, 68, 338-344. (b) Wolff, S.; Agosta, W. J. Org. Chem. 1981, 46, 4821-4825. (c) Rizzo, C. J.; Dunlap, N. K.; Smith, A. B. J. Org. Chem. 1987, 52, 5280-5283.
    • (1985) Helv. Chim. Acta , vol.68 , pp. 338-344
    • Ackroyd, J.1    Karpf, M.2    Dreiding, A.S.3
  • 32
    • 0005768359 scopus 로고
    • 4-Alkylidene-2-cyclopenten-1-ones also have been obtained as reaction byproducts; for example, see: (a) Ackroyd, J.; Karpf, M.; Dreiding, A. S. Helv. Chim. Acta 1985, 68, 338-344. (b) Wolff, S.; Agosta, W. J. Org. Chem. 1981, 46, 4821-4825. (c) Rizzo, C. J.; Dunlap, N. K.; Smith, A. B. J. Org. Chem. 1987, 52, 5280-5283.
    • (1981) J. Org. Chem. , vol.46 , pp. 4821-4825
    • Wolff, S.1    Agosta, W.2
  • 33
    • 0023618571 scopus 로고
    • 4-Alkylidene-2-cyclopenten-1-ones also have been obtained as reaction byproducts; for example, see: (a) Ackroyd, J.; Karpf, M.; Dreiding, A. S. Helv. Chim. Acta 1985, 68, 338-344. (b) Wolff, S.; Agosta, W. J. Org. Chem. 1981, 46, 4821-4825. (c) Rizzo, C. J.; Dunlap, N. K.; Smith, A. B. J. Org. Chem. 1987, 52, 5280-5283.
    • (1987) J. Org. Chem. , vol.52 , pp. 5280-5283
    • Rizzo, C.J.1    Dunlap, N.K.2    Smith, A.B.3
  • 39
    • 0030873573 scopus 로고    scopus 로고
    • The asymmetric Birch reduction-alkylations of a chiral 2-trimethylsilylbenzamide also have been reported; see: (a) Schultz, A. G.; Pettus, L. J. Org. Chem. 1997, 62, 6855-6861. (b) Schultz, A. G.; Pettus, L. Tetrahedron Lett. 1997, 38, 5433-5436.
    • (1997) J. Org. Chem. , vol.62 , pp. 6855-6861
    • Schultz, A.G.1    Pettus, L.2
  • 40
    • 0030792352 scopus 로고    scopus 로고
    • The asymmetric Birch reduction-alkylations of a chiral 2-trimethylsilylbenzamide also have been reported; see: (a) Schultz, A. G.; Pettus, L. J. Org. Chem. 1997, 62, 6855-6861. (b) Schultz, A. G.; Pettus, L. Tetrahedron Lett. 1997, 38, 5433-5436.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5433-5436
    • Schultz, A.G.1    Pettus, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.