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Volumn 49, Issue 18, 2008, Pages 2946-2950

A double ring-closing olefin metathesis approach to [3]catenanes

Author keywords

Catenane; Macrocycle; Pseudorotaxane; Ring closing metathesis

Indexed keywords

ALKENE; CATENANE; COPPER ION; PHENANTHROLINE; PSEUDOROTAXANE; TAXANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 41349089481     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.03.012     Document Type: Article
Times cited : (26)

References (51)
  • 45
    • 41349093785 scopus 로고    scopus 로고
    • note
    • Other approaches to [3]catenanes, for the most part, consist of either a double coupling reaction between two [2]pseudorotaxanes or a single ring-closing reaction of a doubly threaded acyclic precursor, that is, a [3]pseudorotaxane.
  • 49
    • 41349094805 scopus 로고    scopus 로고
    • note
    • See Supplementary data.
  • 51
    • 41349117403 scopus 로고    scopus 로고
    • Recently, Stoddart et al. reported the highest yielding [3]catenane-forming reactions (84% and 91%) to date in iodide-catalysed self-assembly of donor-acceptor [3]catenanes, see: Patel, K.; Miljanić, O. Š.; Stoddart, J. F. Chem. Commun. Advance Articles, first published on the web on the 29th of November, 2007. For high yielding syntheses (67-72%) of metallo[3]catenanes, see Ref. 4a.
    • Recently, Stoddart et al. reported the highest yielding [3]catenane-forming reactions (84% and 91%) to date in iodide-catalysed self-assembly of donor-acceptor [3]catenanes, see: Patel, K.; Miljanić, O. Š.; Stoddart, J. F. Chem. Commun. Advance Articles, first published on the web on the 29th of November, 2007. For high yielding syntheses (67-72%) of metallo[3]catenanes, see Ref. 4a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.