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Volumn , Issue 23, 2006, Pages 5387-5393

Suzuki-Miyaura cross-coupling and ring-closing metathesis: A strategic combination for the synthesis of cyclophane derivatives

Author keywords

Cyclophanes; Isomerization; Olefin metathesis; Palladium; Ruthenium; Suzuki Miyaura cross coupling

Indexed keywords


EID: 33845389865     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200600549     Document Type: Article
Times cited : (32)

References (89)
  • 4
    • 1442360753 scopus 로고    scopus 로고
    • (Ed.: R. H. Grubbs), Wiley-VCH, Wenheim
    • a) Handbook of Metathesis (Ed.: R. H. Grubbs), Wiley-VCH, Wenheim, 2003, vols. 1-3.
    • (2003) Handbook of Metathesis , vol.1-3
  • 13
    • 0141545206 scopus 로고    scopus 로고
    • For some related examples in this area, see: a) D. Banti, M. North, Tetrahedron Lett. 2003, 44, 8157-8160;
    • (2003) Tetrahedron Lett. , vol.44 , pp. 8157-8160
    • Banti, D.1    North, M.2
  • 26
    • 2042507954 scopus 로고
    • For reviews on SM cross-coupling, see: b) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457-2483;
    • (1995) Chem. Rev. , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 34
    • 22944472540 scopus 로고
    • Springer-Verlag, Berlin, Germany
    • a) E. Weber, Cyclophanes, Springer-Verlag, Berlin, Germany, 1994, vol. 172;
    • (1994) Cyclophanes , vol.172
    • Weber, E.1
  • 36
    • 0003825877 scopus 로고
    • Royal Society of Chemistry, Cambridge, UK
    • c) F. Diederich, Cyclophanes, Royal Society of Chemistry, Cambridge, UK, 1991;
    • (1991) Cyclophanes
    • Diederich, F.1
  • 37
    • 16244379157 scopus 로고    scopus 로고
    • H. Takemura (Ed.), Research Signpost, Trivandrum, India
    • st Century, Research Signpost, Trivandrum, India, 2002.
    • (2002) st Century
  • 63
  • 73
    • 33845440162 scopus 로고    scopus 로고
    • note
    • 1H NMR peak intensity ratio) because of their similar polarity. Hence, the purification of these materials was carried out by either repeated column chromatography or repeated crystallizations after column chromatography.
  • 74
    • 33845444261 scopus 로고    scopus 로고
    • note
    • Yield varies from 74 to 85%.
  • 75
    • 33845408704 scopus 로고    scopus 로고
    • note
    • [5].
  • 76
    • 0033582741 scopus 로고    scopus 로고
    • Related examples of Grubbs' catalyst-induced isomerization, see: a) T. R. Hoye, M. A. Promo, Tetrahedron Lett. 1999, 40, 1429-1432;
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1429-1432
    • Hoye, T.R.1    Promo, M.A.2
  • 87


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.