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Volumn 52, Issue 30, 1996, Pages 10113-10130

On the efficiency of tetraalkylammonium salts in Heck type reactions

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLIC ACID DERIVATIVE;

EID: 0030598098     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00547-9     Document Type: Article
Times cited : (592)

References (64)
  • 1
    • 0000702671 scopus 로고
    • and references cited therein
    • 1. (a) Heck, R. F. Org. React. 1982, 27, 345-390 and references cited therein.
    • (1982) Org. React. , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 3
    • 0000633011 scopus 로고
    • Trost, B. M.; Fleming, I. Eds; Pergamon Press: Oxford, New York, and references cited therein
    • (c) Heck, R. F. in Comprehensive Organic Synthesis, Trost, B. M.; Fleming, I. Eds; Pergamon Press: Oxford, New York, 1991, Vol 4; pp. 833-863 and references cited therein.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 833-863
    • Heck, R.F.1
  • 11
    • 84993869046 scopus 로고
    • and references cited therein
    • (b) Grigg, R. J. Heterocycl. Chem. 1994, 31, 631-639 and references cited therein.
    • (1994) Heterocycl. Chem. , vol.31 , pp. 631-639
    • Grigg, R.J.1
  • 12
    • 0038584673 scopus 로고
    • and references cited therein
    • (c) Cabri, W.; Candiani, I. Acc. Chem. Res. 1995, 28, 2-7 and references cited therein.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 2-7
    • Cabri, W.1    Candiani, I.2
  • 13
    • 0001390892 scopus 로고    scopus 로고
    • Liebeskind, L. S. Ed.; JAI Press: Greenwich CT, and references cited therein
    • (d) Jeffery, T. in Advances in Metal-Organic Chemistry, Liebeskind, L. S. Ed.; JAI Press: Greenwich CT, 1996, Vol 5; pp. 149-256 and references cited therein.
    • (1996) Advances in Metal-Organic Chemistry , vol.5 , pp. 149-256
    • Jeffery, T.1
  • 54
    • 85030208771 scopus 로고    scopus 로고
    • Both hydrated and non hydrated tetra-n-butylammonium chloride are now commercially available (for example as "tetrabutylammonium chloride hydrate 98%" (from Aldrich) and "tetra-n-butylammonium chloride 98%" from Lancaster). Up to about five years ago, the products were all labelled as "tetrabutylammonium chloride" or "tetrabutylammonium chloride, tech.", but very probably were all hydrated salts as only very moist solids were available
    • 7. Both hydrated and non hydrated tetra-n-butylammonium chloride are now commercially available (for example as "tetrabutylammonium chloride hydrate 98%" (from Aldrich) and "tetra-n-butylammonium chloride 98%" from Lancaster). Up to about five years ago, the products were all labelled as "tetrabutylammonium chloride" or "tetrabutylammonium chloride, tech.", but very probably were all hydrated salts as only very moist solids were available.
  • 56
    • 85030201738 scopus 로고    scopus 로고
    • 10
    • 10
  • 64
    • 0012020375 scopus 로고
    • VCH: Weinheim, New York, 3rd ed., and references cited therein
    • (e) Dehmlow; E. V.; Dehmlow; S. S. Phase Transfer Catalysts, VCH: Weinheim, New York, 3rd ed., 1993 and references cited therein.
    • (1993) Phase Transfer Catalysts
    • Dehmlow, E.V.1    Dehmlow, S.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.