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Volumn 73, Issue 6, 2008, Pages 2345-2356

Preparation and intramolecular [2+2]-photocycloaddition of 1,5-dihydropyrrol-2-ones and 5,6-dihydro-1H-pyridin-2-ones with C-, N-, and O-linked alkenyl side chains at the 4-position

Author keywords

[No Author keywords available]

Indexed keywords

ACIDS; DERIVATIVES; NUCLEAR MAGNETIC RESONANCE; PYRIDINE; REACTION KINETICS;

EID: 41849104720     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7027129     Document Type: Article
Times cited : (46)

References (130)
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    • For general reviews on [2+2]-photocycloaddition reactions, see: (a) Fleming, S. A. In Molecular and Supramolecular Photochemistry: Synthetic Organic Photochemistry; Griesbeck, A. G., Mattay, J., Eds.; Dekker: New York, 2005; 12, pp 141-160.
    • For general reviews on [2+2]-photocycloaddition reactions, see: (a) Fleming, S. A. In Molecular and Supramolecular Photochemistry: Synthetic Organic Photochemistry; Griesbeck, A. G., Mattay, J., Eds.; Dekker: New York, 2005; Vol. 12, pp 141-160.
  • 7
    • 41849110162 scopus 로고    scopus 로고
    • For reviews of mechanistic studies on [2+2]-photocycloaddition reactions, see: (a) Schuster, D. I. In CRC Handbook of Organic Photochemistry and Photobiology; 2nd ed.; Horspool, W. M., Lend, F., Eds.; CRC Press: Boca Raton, FL, 2004; pp 72.1-72.24.
    • For reviews of mechanistic studies on [2+2]-photocycloaddition reactions, see: (a) Schuster, D. I. In CRC Handbook of Organic Photochemistry and Photobiology; 2nd ed.; Horspool, W. M., Lend, F., Eds.; CRC Press: Boca Raton, FL, 2004; pp 72.1-72.24.
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    • (d) Mattay, J.; Conrads, R.; Hoffmann, R. In Houben-Weyl Methods of Organic Chemistry, 4th ed.; Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: Stuttgart, 1995; Vol. E 21c, pp 3085-3132.
    • (1995) Houben-Weyl Methods of Organic Chemistry , vol.E 21c , pp. 3085-3132
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    • 0013548984 scopus 로고    scopus 로고
    • For intramolecular [2+2]-photocycloadditons of non-aromatic α,β-unsatured lactones, see: (a) Coates, R. M.; Muskopf, J. W.; Senter, P. A. J. Org. Chem. 1985, 50, 3541-3557.
    • For intramolecular [2+2]-photocycloadditons of non-aromatic α,β-unsatured lactones, see: (a) Coates, R. M.; Muskopf, J. W.; Senter, P. A. J. Org. Chem. 1985, 50, 3541-3557.
  • 24
    • 0012545891 scopus 로고    scopus 로고
    • For intramolecular [2+2]-photocycloadditons of non-aromatic α,β-unsatured lactams, see: (a) Wrobel, M. N.; Margaretha, P. Chem. Commun. 1998, 541-542.
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  • 41
    • 0011237795 scopus 로고
    • For similar reactions of tetronic acid bromide derivatives and amines, see: a
    • For similar reactions of tetronic acid bromide derivatives and amines, see: (a) Farina, F.; Martín, M. V.; Sánchez, F.; Maestro, M. C.; Martín, M. R. Synthesis 1983, 5, 397-398.
    • (1983) Synthesis , vol.5 , pp. 397-398
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  • 46
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    • For aminodehydroxylations of tetronic acids, see inter alia: (a) Schick, H.; Gründemann, E.; Ballschuh, D. J. Prakt. Chem. 1980, 322, 559-568.
    • For aminodehydroxylations of tetronic acids, see inter alia: (a) Schick, H.; Gründemann, E.; Ballschuh, D. J. Prakt. Chem. 1980, 322, 559-568.
  • 79
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    • Huo, S.1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.