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Volumn 22, Issue 13, 2003, Pages 1665-1671

The retro-chloropalladation reaction of heterosubstituted alkynes

Author keywords

Alkynes; Monomeric compounds; Propargyl amines; Retro chloropalladation reaction

Indexed keywords

AMINES; LIGANDS; PALLADIUM COMPOUNDS;

EID: 0038573753     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0277-5387(03)00324-3     Document Type: Article
Times cited : (14)

References (26)
  • 4
    • 0035886138 scopus 로고    scopus 로고
    • For recent reviews of palladacycles see: (a) M. Albrecht, G. van Koten, Angew. Chem., Int. Ed. 40 (2001) 3750. (b) J. Dupont, M. Pfeffer, J. Spencer, Eur. J. Inorg. Chem. (2001) 1917.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 3750
    • Albrecht, M.1    Van Koten, G.2
  • 5
    • 0034928699 scopus 로고    scopus 로고
    • For recent reviews of palladacycles see: (a) M. Albrecht, G. van Koten, Angew. Chem., Int. Ed. 40 (2001) 3750. (b) J. Dupont, M. Pfeffer, J. Spencer, Eur. J. Inorg. Chem. (2001) 1917.
    • (2001) Eur. J. Inorg. Chem. , pp. 1917
    • Dupont, J.1    Pfeffer, M.2    Spencer, J.3
  • 15
    • 0008095522 scopus 로고
    • The action of isonitriles with palladacycles usually results in insertion of these unsaturated molecules into the Pd-C bond. See for example: (a) J. Dupont, M. Pfeffer, J.C. Daran, Y. Jeannin, Organometallics 6 (1987) 899. (b) J. Dupont, M. Pfeffer, J. Chem. Soc., Dalton Trans. (1990) 3193.
    • (1987) Organometallics , vol.6 , pp. 899
    • Dupont, J.1    Pfeffer, M.2    Daran, J.C.3    Jeannin, Y.4
  • 16
    • 37049075398 scopus 로고
    • The action of isonitriles with palladacycles usually results in insertion of these unsaturated molecules into the Pd-C bond. See for example: (a) J. Dupont, M. Pfeffer, J.C. Daran, Y. Jeannin, Organometallics 6 (1987) 899. (b) J. Dupont, M. Pfeffer, J. Chem. Soc., Dalton Trans. (1990) 3193.
    • (1990) J. Chem. Soc., Dalton Trans. , pp. 3193
    • Dupont, J.1    Pfeffer, M.2
  • 18
    • 51149219999 scopus 로고
    • The Pd-C of 'classical' palladacycles usually undergoes insertion reactions with these unsaturated reagents. See for example: (a) J. Dupont, M. Pfeffer, J.C. Daran, J. Gouteron, J. Chem. Soc., Dalton Trans. (1988) 2421. (b) M. Pfeffer, Rec. Trav. Chim. Pay.Bas. 109 (1990) 567.
    • (1988) J. Chem. Soc., Dalton Trans. , pp. 2421
    • Dupont, J.1    Pfeffer, M.2    Daran, J.C.3    Gouteron, J.4
  • 19
    • 84987064271 scopus 로고
    • The Pd-C of 'classical' palladacycles usually undergoes insertion reactions with these unsaturated reagents. See for example: (a) J. Dupont, M. Pfeffer, J.C. Daran, J. Gouteron, J. Chem. Soc., Dalton Trans. (1988) 2421. (b) M. Pfeffer, Rec. Trav. Chim. Pay.Bas. 109 (1990) 567.
    • (1990) Rec. Trav. Chim. Pay. Bas. , vol.109 , pp. 567
    • Pfeffer, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.