메뉴 건너뛰기




Volumn , Issue 9, 2003, Pages 1722-1728

Synthesis of maleic anhydrides and maleic acids by Pd-catalyzed oxidative dicarbonylation of alk-1-ynes

Author keywords

Anhydrides; Carbonylation; Maleic acids; Palladium

Indexed keywords

ALKYNE; CARBON DIOXIDE; CARBONYL DERIVATIVE; MALEIC ACID DERIVATIVE; MALEIC ANHYDRIDE; PALLADIUM; WATER;

EID: 0037989844     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200210706     Document Type: Article
Times cited : (56)

References (51)
  • 1
    • 0037048517 scopus 로고    scopus 로고
    • For some recent examples of synthesis of 2 by non-carbonylative approaches, see: [1a] A. Kar, N. P. Argade, Tetrahedron Lett. 2002, 43, 6563-6564. [1b] R. M. Adlington, J. E. Baldwin, R. J. Cox, G. J. Pritchard, Synlett 2002, 820-822. [1c] E. M. Beccalli, M. L. Gelmi, A. Marchesini, Eur. J. Org. Chem. 1999, 1421-1426.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 6563-6564
    • Kar, A.1    Argade, N.P.2
  • 2
    • 0036250832 scopus 로고    scopus 로고
    • For some recent examples of synthesis of 2 by non-carbonylative approaches, see: [1a] A. Kar, N. P. Argade, Tetrahedron Lett. 2002, 43, 6563-6564. [1b] R. M. Adlington, J. E. Baldwin, R. J. Cox, G. J. Pritchard, Synlett 2002, 820-822. [1c] E. M. Beccalli, M. L. Gelmi, A. Marchesini, Eur. J. Org. Chem. 1999, 1421-1426.
    • (2002) Synlett , pp. 820-822
    • Adlington, R.M.1    Baldwin, J.E.2    Cox, R.J.3    Pritchard, G.J.4
  • 3
    • 0032770722 scopus 로고    scopus 로고
    • For some recent examples of synthesis of 2 by non-carbonylative approaches, see: [1a] A. Kar, N. P. Argade, Tetrahedron Lett. 2002, 43, 6563-6564. [1b] R. M. Adlington, J. E. Baldwin, R. J. Cox, G. J. Pritchard, Synlett 2002, 820-822. [1c] E. M. Beccalli, M. L. Gelmi, A. Marchesini, Eur. J. Org. Chem. 1999, 1421-1426.
    • (1999) Eur. J. Org. Chem. , pp. 1421-1426
    • Beccalli, E.M.1    Gelmi, M.L.2    Marchesini, A.3
  • 4
    • 15444343493 scopus 로고    scopus 로고
    • Maleic anhydrides can be useful precursors for the preparation of succinic anhydrides, which are important intermediates for the preparation of biologically active molecules. For some recent examples, see: [2a] D. E. Levy, F. Lapierre, W. Liang, W. Ye, C. W. Lange, X. Li, D. Grobelny, M. Casabonne, D. Tyrrel, K. Holme, A. Nadzan, R. E. Galardy, J. Med. Chem. 1998, 41, 199-223. [2b] N. A. Porter, D. M. Scott, I. J. Rosenstein, B. Giese, A. Veit, H. G. Zeitz, J. Am. Chem. Soc. 1991, 113, 1791-1799. [2c] W. C. Groutas, M. J. Brubaker, M. A. Stanga, J. C. Castrisos, J. P. Crowley, E. J. Schatz, J. Med. Chem. 1989, 32, 1607-1611.
    • (1998) J. Med. Chem. , vol.41 , pp. 199-223
    • Levy, D.E.1    Lapierre, F.2    Liang, W.3    Ye, W.4    Lange, C.W.5    Li, X.6    Grobelny, D.7    Casabonne, M.8    Tyrrel, D.9    Holme, K.10    Nadzan, A.11    Galardy, R.E.12
  • 5
    • 0001586445 scopus 로고
    • Maleic anhydrides can be useful precursors for the preparation of succinic anhydrides, which are important intermediates for the preparation of biologically active molecules. For some recent examples, see: [2a] D. E. Levy, F. Lapierre, W. Liang, W. Ye, C. W. Lange, X. Li, D. Grobelny, M. Casabonne, D. Tyrrel, K. Holme, A. Nadzan, R. E. Galardy, J. Med. Chem. 1998, 41, 199-223. [2b] N. A. Porter, D. M. Scott, I. J. Rosenstein, B. Giese, A. Veit, H. G. Zeitz, J. Am. Chem. Soc. 1991, 113, 1791-1799. [2c] W. C. Groutas, M. J. Brubaker, M. A. Stanga, J. C. Castrisos, J. P. Crowley, E. J. Schatz, J. Med. Chem. 1989, 32, 1607-1611.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 1791-1799
    • Porter, N.A.1    Scott, D.M.2    Rosenstein, I.J.3    Giese, B.4    Veit, A.5    Zeitz, H.G.6
  • 6
    • 0024333382 scopus 로고
    • Maleic anhydrides can be useful precursors for the preparation of succinic anhydrides, which are important intermediates for the preparation of biologically active molecules. For some recent examples, see: [2a] D. E. Levy, F. Lapierre, W. Liang, W. Ye, C. W. Lange, X. Li, D. Grobelny, M. Casabonne, D. Tyrrel, K. Holme, A. Nadzan, R. E. Galardy, J. Med. Chem. 1998, 41, 199-223. [2b] N. A. Porter, D. M. Scott, I. J. Rosenstein, B. Giese, A. Veit, H. G. Zeitz, J. Am. Chem. Soc. 1991, 113, 1791-1799. [2c] W. C. Groutas, M. J. Brubaker, M. A. Stanga, J. C. Castrisos, J. P. Crowley, E. J. Schatz, J. Med. Chem. 1989, 32, 1607-1611.
    • (1989) J. Med. Chem. , vol.32 , pp. 1607-1611
    • Groutas, W.C.1    Brubaker, M.J.2    Stanga, M.A.3    Castrisos, J.C.4    Crowley, J.P.5    Schatz, E.J.6
  • 8
  • 10
    • 0033069679 scopus 로고    scopus 로고
    • For some recent examples, see: [4a] P. Nuhn, A. Herrmann, M. Radman, Pharmazie 1999, 54, 93-98. [4b] R. M. Slade, B. P. Branchaud, J. Org. Chem. 1998, 63, 3544-3549. [4c] E. S. Ratemi, J. M. Dolence, C. D. Poulter, J. C. Vederas, J. Org. Chem. 1996, 61, 6296-6301. [4d] R. A. Bit, P. D. Davis, L. H. Elliott, W. Harris, C. H. Hill, E. Keech, H. Kumar, G. Lawton, A. Maw, J. S. Nixon, D. R. Vesey, J. Wadsworth, S. E. Wilkinson, J. Med. Chem. 1993, 36, 21-29. [4e] G. Pattenden, M. W. Turvill, A. P. Chorlton, J. Chem. Soc., Perkin Trans. 1 1991, 2357-2361.
    • (1999) Pharmazie , vol.54 , pp. 93-98
    • Nuhn, P.1    Herrmann, A.2    Radman, M.3
  • 11
    • 0032577623 scopus 로고    scopus 로고
    • For some recent examples, see: [4a] P. Nuhn, A. Herrmann, M. Radman, Pharmazie 1999, 54, 93-98. [4b] R. M. Slade, B. P. Branchaud, J. Org. Chem. 1998, 63, 3544-3549. [4c] E. S. Ratemi, J. M. Dolence, C. D. Poulter, J. C. Vederas, J. Org. Chem. 1996, 61, 6296-6301. [4d] R. A. Bit, P. D. Davis, L. H. Elliott, W. Harris, C. H. Hill, E. Keech, H. Kumar, G. Lawton, A. Maw, J. S. Nixon, D. R. Vesey, J. Wadsworth, S. E. Wilkinson, J. Med. Chem. 1993, 36, 21-29. [4e] G. Pattenden, M. W. Turvill, A. P. Chorlton, J. Chem. Soc., Perkin Trans. 1 1991, 2357-2361.
    • (1998) J. Org. Chem. , vol.63 , pp. 3544-3549
    • Slade, R.M.1    Branchaud, B.P.2
  • 12
    • 0029833497 scopus 로고    scopus 로고
    • For some recent examples, see: [4a] P. Nuhn, A. Herrmann, M. Radman, Pharmazie 1999, 54, 93-98. [4b] R. M. Slade, B. P. Branchaud, J. Org. Chem. 1998, 63, 3544-3549. [4c] E. S. Ratemi, J. M. Dolence, C. D. Poulter, J. C. Vederas, J. Org. Chem. 1996, 61, 6296-6301. [4d] R. A. Bit, P. D. Davis, L. H. Elliott, W. Harris, C. H. Hill, E. Keech, H. Kumar, G. Lawton, A. Maw, J. S. Nixon, D. R. Vesey, J. Wadsworth, S. E. Wilkinson, J. Med. Chem. 1993, 36, 21-29. [4e] G. Pattenden, M. W. Turvill, A. P. Chorlton, J. Chem. Soc., Perkin Trans. 1 1991, 2357-2361.
    • (1996) J. Org. Chem. , vol.61 , pp. 6296-6301
    • Ratemi, E.S.1    Dolence, J.M.2    Poulter, C.D.3    Vederas, J.C.4
  • 14
    • 37049073303 scopus 로고
    • For some recent examples, see: [4a] P. Nuhn, A. Herrmann, M. Radman, Pharmazie 1999, 54, 93-98. [4b] R. M. Slade, B. P. Branchaud, J. Org. Chem. 1998, 63, 3544-3549. [4c] E. S. Ratemi, J. M. Dolence, C. D. Poulter, J. C. Vederas, J. Org. Chem. 1996, 61, 6296-6301. [4d] R. A. Bit, P. D. Davis, L. H. Elliott, W. Harris, C. H. Hill, E. Keech, H. Kumar, G. Lawton, A. Maw, J. S. Nixon, D. R. Vesey, J. Wadsworth, S. E. Wilkinson, J. Med. Chem. 1993, 36, 21-29. [4e] G. Pattenden, M. W. Turvill, A. P. Chorlton, J. Chem. Soc., Perkin Trans. 1 1991, 2357-2361.
    • (1991) J. Chem. Soc., Perkin Trans. 1 , pp. 2357-2361
    • Pattenden, G.1    Turvill, M.W.2    Chorlton, A.P.3
  • 44
    • 0003002540 scopus 로고    scopus 로고
    • and references therein
    • X. Yin, J. R. Moss, Coord. Chem. Rev. 1999, 181, 27-59 and references therein.
    • (1999) Coord. Chem. Rev. , vol.181 , pp. 27-59
    • Yin, X.1    Moss, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.