메뉴 건너뛰기




Volumn , Issue 16, 2003, Pages 2530-2534

Synthesis of Geminal Dimetal-Substituted Terminal Alkenes Utilizing a Cuprate Rearrangement: Toward an Efficient and General Access to Trisubstituted Olefins

Author keywords

Copper; Lithium; Metalate rearrangement; Tin; Trisubstituted olefins

Indexed keywords

FURAN RESINS; QUENCHING; STEREOCHEMISTRY; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 0345305264     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-42445     Document Type: Article
Times cited : (10)

References (29)
  • 19
    • 0011274954 scopus 로고
    • + quench, the distannyl 15 was formed in less than 2% yield. Formation of a ditin compound was earlier reported during a stannylcupration followed by trappping with an electrophile other than proton, see: (a) Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1602. (b) See also: Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1604. (c) See also: Betzer, J. F.; Delaloge, F.; Muller, B.; Pancrazi, A.; Prunet, J. J. Org. Chem. 1997, 62, 7768. (d) Suzenet, F.; Blart, E.; Quintard, J.-P. Synlett 1998, 879.
    • (1982) J. Org. Chem. , vol.47 , pp. 1602
    • Piers, E.1    Chong, J.M.2
  • 20
    • 0345508330 scopus 로고
    • + quench, the distannyl 15 was formed in less than 2% yield. Formation of a ditin compound was earlier reported during a stannylcupration followed by trappping with an electrophile other than proton, see: (a) Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1602. (b) See also: Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1604. (c) See also: Betzer, J. F.; Delaloge, F.; Muller, B.; Pancrazi, A.; Prunet, J. J. Org. Chem. 1997, 62, 7768. (d) Suzenet, F.; Blart, E.; Quintard, J.-P. Synlett 1998, 879.
    • (1982) J. Org. Chem. , vol.47 , pp. 1604
    • Piers, E.1    Chong, J.M.2
  • 21
    • 0001422640 scopus 로고    scopus 로고
    • + quench, the distannyl 15 was formed in less than 2% yield. Formation of a ditin compound was earlier reported during a stannylcupration followed by trappping with an electrophile other than proton, see: (a) Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1602. (b) See also: Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1604. (c) See also: Betzer, J. F.; Delaloge, F.; Muller, B.; Pancrazi, A.; Prunet, J. J. Org. Chem. 1997, 62, 7768. (d) Suzenet, F.; Blart, E.; Quintard, J.-P. Synlett 1998, 879.
    • (1997) J. Org. Chem. , vol.62 , pp. 7768
    • Betzer, J.F.1    Delaloge, F.2    Muller, B.3    Pancrazi, A.4    Prunet, J.5
  • 22
    • 0001817631 scopus 로고    scopus 로고
    • + quench, the distannyl 15 was formed in less than 2% yield. Formation of a ditin compound was earlier reported during a stannylcupration followed by trappping with an electrophile other than proton, see: (a) Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1602. (b) See also: Piers, E.; Chong, J. M. J. Org. Chem. 1982, 47, 1604. (c) See also: Betzer, J. F.; Delaloge, F.; Muller, B.; Pancrazi, A.; Prunet, J. J. Org. Chem. 1997, 62, 7768. (d) Suzenet, F.; Blart, E.; Quintard, J.-P. Synlett 1998, 879.
    • (1998) Synlett , pp. 879
    • Suzenet, F.1    Blart, E.2    Quintard, J.-P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.