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Volumn 10, Issue 13, 2004, Pages 3324-3330

Rational synthesis of multicyclic bis[2]catenanes

Author keywords

Calixarenes; Catenanes; Hydrogen bonds; Metathesis; Seff assembly

Indexed keywords

ACYLATION; DIMERS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROGENATION; MIXTURES; ORGANIC SOLVENTS; STOICHIOMETRY; SYNTHESIS (CHEMICAL);

EID: 3142697833     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200400195     Document Type: Article
Times cited : (68)

References (54)
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    • note
    • The presence of a suitable guest is necessary for the formation of dimeric capsules. In this case this is the solvent and will not be mentioned further.
  • 41
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    • note
    • Preorganization of alkenyl substituted molecules through hydrogen bonding was also used in other cases for a topologically correct covalent linkage by metathesis, see: ref. [12a, 14a,b, 15].
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    • Catenanes and knots have been prepared by metathesis using also the preorganization by π-π stacking and by metal coordination: a) D. G. Hamilton, N. Feeder, S. J. Teat, J. K. M. Sanders, New J. Chem. 1998, 22, 1019-1021;
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    • Hamilton, D.G.1    Feeder, N.2    Teat, S.J.3    Sanders, J.K.M.4
  • 45
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    • note
    • Bis[2]catenanes of type 2 may be considered not only as two macrocyclic molecules (the two calix[4]arenes) connected in a (macro)cyclic way by two [2]catenane structures or as two [2]catenanes connected to a macrocycle by two times two bridges (A). Their overall structure may also be regarded as a doubly interlocked [2]catenane having additionally two bridges within each ring (B). (Diagram presented).
  • 46
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    • note
    • By A and B phenolic units differing by their ether or/and urea residues Y and R are characterized.
  • 50
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    • note
    • This principle was used by Sauvage et al. for the Cu(I)-templated synthesis of catenanes, where equimolar amounts of acyclic and open-chain phenanthroline derivatives form only hetero complexes for the same reason, see ref. [7].
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    • note
    • When "activated" by the catalyst, 50% of the alkenyl groups can undergo only α-connections, whereas the other 50% have a 1:1 chance to make α- or β-connections.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.