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Volumn 19, Issue 8, 2000, Pages 1458-1460

Palladium-catalyzed carboxylative coupling of allylstannanes and allyl halides

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; ORGANOMETALLICS; PALLADIUM; PLATINUM;

EID: 0033742717     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om0000966     Document Type: Article
Times cited : (77)

References (30)
  • 1
  • 7
    • 33646315593 scopus 로고    scopus 로고
    • note
    • 2 with 1,3-dienes and alkynes, which likely proceed via metal-carboxylate intermediates, often produce esters or lactones; for reviews and lead references, see ref 1c, pp 94-96 and 106-129.
  • 13
    • 33646318824 scopus 로고    scopus 로고
    • note
    • 2 three times and then pressurized to 750 psig. The system was then heated at 70 °C for 48 h. After cooling, the autoclave was vented, the solvent was removed by rotary evaporation, and the ester products were isolated by Kugelrohr distillation. In some runs naphthalene was added as an internal standard; samples were withdrawn periodically via a dip tube and analyzed by GC. Spectroscopic data for ester 3a are included in the Supporting Information.
  • 22
    • 33646313706 scopus 로고
    • Dissertation, Ruhr-Universitat, Bochum, Germany
    • (b) Hung, T. Dissertation, Ruhr-Universitat, Bochum, Germany, 1980.
    • (1980)
    • Hung, T.1
  • 25
    • 0030755285 scopus 로고    scopus 로고
    • A similar scheme has been proposed for the recently reported Pd-catalyzed three-component coupling of allylstannanes, allyl halides, and electrophilic alkenes: Nakamura, H.; Shim, J.-G.; Yamamoto, Y. J. Am. Chem. Soc. 1997, 119, 8113.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8113
    • Nakamura, H.1    Shim, J.-G.2    Yamamoto, Y.3
  • 27
    • 33646284570 scopus 로고    scopus 로고
    • note
    • 119Sn NMR spectra with those of authentic samples.
  • 28
    • 33646324923 scopus 로고    scopus 로고
    • note
    • The identities of esters 3a-d were established by GC/MS and NMR analysis of the mixture and by comparison with authentic samples of each ester, which were prepared by DCC-DMAP-promoted reactions of the respective carboxylic acids and alcohols. Spectral data for 3a-d are available in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.