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Volumn 59, Issue 2, 2003, Pages 669-684

The photodecarboxylative addition of carboxylates to phthalimides: Scope and limitations

Author keywords

[No Author keywords available]

Indexed keywords

1 ADAMANTANECARBOXYLIC ACID; CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; HYDROXYPHTHALIMIDE DERIVATIVE; PHTHALIMIDE DERIVATIVE; POTASSIUM; UNCLASSIFIED DRUG;

EID: 0037344547     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-02-S77     Document Type: Article
Times cited : (38)

References (50)
  • 1
    • 33947093639 scopus 로고
    • For early reviews, see: a) Y. Kanaoka, Acc. Chem. Res., 1978, 11, 407; b) Y. Kanaoka, J Synth. Org. Chem. Jpn., 1975, 33, 949.
    • (1978) Acc. Chem. Res. , vol.11 , pp. 407
    • Kanaoka, Y.1
  • 2
    • 85010143875 scopus 로고
    • For early reviews, see: a) Y. Kanaoka, Acc. Chem. Res., 1978, 11, 407; b) Y. Kanaoka, J Synth. Org. Chem. Jpn., 1975, 33, 949.
    • (1975) J. Synth. Org. Chem. Jpn. , vol.33 , pp. 949
    • Kanaoka, Y.1
  • 4
    • 0002123059 scopus 로고
    • Ed. by W. M. Horspool, Plenum Press, New York
    • b) J. D. Coyle, 'Synthetic Organic Photochemistry', ed. by W. M. Horspool, Plenum Press, New York, 1984, pp. 259-284;
    • (1984) Synthetic Organic Photochemistry , pp. 259-284
    • Coyle, J.D.1
  • 28
    • 0033536703 scopus 로고    scopus 로고
    • Yoon and Mariano recently described the formation of decarboxylation products in moderate yields during the photolysis of 6 in acetonitrile: U. C. Yoon, C. W. Lee, S. W. Oh, and P. S. Mariano, Tetrahedron, 1999, 55, 11997.
    • (1999) Tetrahedron , vol.55 , pp. 11997
    • Yoon, U.C.1    Lee, C.W.2    Oh, S.W.3    Mariano, P.S.4
  • 33
    • 0036070731 scopus 로고    scopus 로고
    • For further examples of this concept, see: a) A. G. Griesbeck and A. Bartoschek, Chem. Commun., 2002, 1594; b) C. Schiel, M. Oelgemöller, J. Ortner, and J. Mattay, Green Chem., 2001, 3, 224; c) A. Albini, M. Fagnoni, and M. Mella, Pure Appl. Chem., 2000, 72, 1321.
    • (2002) Chem. Commun. , pp. 1594
    • Griesbeck, A.G.1    Bartoschek, A.2
  • 34
    • 57249100436 scopus 로고    scopus 로고
    • For further examples of this concept, see: a) A. G. Griesbeck and A. Bartoschek, Chem. Commun., 2002, 1594; b) C. Schiel, M. Oelgemöller, J. Ortner, and J. Mattay, Green Chem., 2001, 3, 224; c) A. Albini, M. Fagnoni, and M. Mella, Pure Appl. Chem., 2000, 72, 1321.
    • (2001) Green Chem. , vol.3 , pp. 224
    • Schiel, C.1    Oelgemöller, M.2    Ortner, J.3    Mattay, J.4
  • 35
    • 0034583290 scopus 로고    scopus 로고
    • For further examples of this concept, see: a) A. G. Griesbeck and A. Bartoschek, Chem. Commun., 2002, 1594; b) C. Schiel, M. Oelgemöller, J. Ortner, and J. Mattay, Green Chem., 2001, 3, 224; c) A. Albini, M. Fagnoni, and M. Mella, Pure Appl. Chem., 2000, 72, 1321.
    • (2000) Pure Appl. Chem. , vol.72 , pp. 1321
    • Albini, A.1    Fagnoni, M.2    Mella, M.3


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