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Volumn 3, Issue 1, 2005, Pages 172-184

1,3-Alternate calix[4]arenes, selectively functionalized by amino groups

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CONFORMATIONS; DERIVATIVES; HYDROGENATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHENOLS; RARE EARTH ELEMENTS; STRUCTURE (COMPOSITION); SYNTHESIS (CHEMICAL); UREA;

EID: 11844272569     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b414173c     Document Type: Article
Times cited : (25)

References (55)
  • 1
    • 0004287470 scopus 로고    scopus 로고
    • Kluwer Academic Publishers, Dordrecht
    • For reviews on calixarenes see:(a) Calixarenes 2001, ed. V. Böhmen, Z. Asfari, J. Harrowfield, J. Vicens, Kluwer Academic Publishers, Dordrecht, 2001.: (b) C. D. Gutsche in Calixarenes Revisited, ed. J. F. Stoddart, The Royal Society of Chemistry, Cambridge, 1998.; (c) V. Böhmer, Angew. Chem., 1995, 107, 785-818; V. Böhmer, Angew. Chem., Int. Ed. Engl., 1995, 34, 713-745.
    • (2001) Calixarenes 2001
    • Böhmen, V.1    Asfari, Z.2    Harrowfield, J.3    Vicens, J.4
  • 2
    • 0004268367 scopus 로고    scopus 로고
    • ed. J. F. Stoddart, The Royal Society of Chemistry, Cambridge
    • For reviews on calixarenes see:(a) Calixarenes 2001, ed. V. Böhmen, Z. Asfari, J. Harrowfield, J. Vicens, Kluwer Academic Publishers, Dordrecht, 2001.: (b) C. D. Gutsche in Calixarenes Revisited, ed. J. F. Stoddart, The Royal Society of Chemistry, Cambridge, 1998.; (c) V. Böhmer, Angew. Chem., 1995, 107, 785-818; V. Böhmer, Angew. Chem., Int. Ed. Engl., 1995, 34, 713-745.
    • (1998) Calixarenes Revisited
    • Gutsche, C.D.1
  • 3
    • 0000948055 scopus 로고
    • For reviews on calixarenes see:(a) Calixarenes 2001, ed. V. Böhmen, Z. Asfari, J. Harrowfield, J. Vicens, Kluwer Academic Publishers, Dordrecht, 2001.: (b) C. D. Gutsche in Calixarenes Revisited, ed. J. F. Stoddart, The Royal Society of Chemistry, Cambridge, 1998.; (c) V. Böhmer, Angew. Chem., 1995, 107, 785-818; V. Böhmer, Angew. Chem., Int. Ed. Engl., 1995, 34, 713-745.
    • (1995) Angew. Chem. , vol.107 , pp. 785-818
    • Böhmer, V.1
  • 4
    • 33748539998 scopus 로고
    • For reviews on calixarenes see:(a) Calixarenes 2001, ed. V. Böhmen, Z. Asfari, J. Harrowfield, J. Vicens, Kluwer Academic Publishers, Dordrecht, 2001.: (b) C. D. Gutsche in Calixarenes Revisited, ed. J. F. Stoddart, The Royal Society of Chemistry, Cambridge, 1998.; (c) V. Böhmer, Angew. Chem., 1995, 107, 785-818; V. Böhmer, Angew. Chem., Int. Ed. Engl., 1995, 34, 713-745.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 713-745
    • Böhmer, V.1
  • 34
    • 11844270620 scopus 로고    scopus 로고
    • note
    • 2 via azides see ref. 10.
  • 37
    • 11844274009 scopus 로고    scopus 로고
    • note
    • 3 the cone isomer is formed as main product.
  • 38
    • 11844288465 scopus 로고    scopus 로고
    • Similar experiences were made with a mixed tetraether in the cone conformation, where both phthalimide groups were hydrolyzed to the monoamide: P. Wang and V. Böhmer, unpublished
    • Similar experiences were made with a mixed tetraether in the cone conformation, where both phthalimide groups were hydrolyzed to the monoamide: P. Wang and V. Böhmer, unpublished.
  • 39
    • 11844252197 scopus 로고    scopus 로고
    • These conditions were successfully applied for monocyano-hepthyloxy surrounded by tripropyloxy residue attached to calixarenes by Y. Rudzevich and V. Böhmer, unpublished results
    • These conditions were successfully applied for monocyano-hepthyloxy surrounded by tripropyloxy residue attached to calixarenes by Y. Rudzevich and V. Böhmer, unpublished results.
  • 43
    • 11844266056 scopus 로고    scopus 로고
    • note
    • The use of bromoalkyl phthalimides or bromonitriles in the first O-alkylation step leads to hexaamines with two amino groups attached to the narrow rim.
  • 45
    • 11844255872 scopus 로고    scopus 로고
    • A tetra-CMPO derivative could be obtained from 28 (n = 3) in three steps by acylation, cleavage of the phthalimide groups and acylation again: C. Danila and V. Böhmer, unpublished
    • A tetra-CMPO derivative could be obtained from 28 (n = 3) in three steps by acylation, cleavage of the phthalimide groups and acylation again: C. Danila and V. Böhmer, unpublished.
  • 46
    • 11844305120 scopus 로고    scopus 로고
    • note
    • Tetraethers in the cow-conformation can be obtained much more selectively.
  • 48
    • 0345736841 scopus 로고    scopus 로고
    • Calixarencs, ed. Z. Rappoport, Wiley, Chichester
    • V. Böhmer in Calixarencs, The Chemistry of Phenols, ed. Z. Rappoport, Wiley, Chichester, 2003.
    • (2003) The Chemistry of Phenols
    • Böhmer, V.1
  • 49
    • 11844258960 scopus 로고    scopus 로고
    • note
    • Since starting point and direction are in principle arbitrary, the sequence (+,-)(+,-)(-,-)(+,+) is identical to (-,+) (+,+)(-,-)(-.+), listed in Table 1.
  • 50
    • 0003433022 scopus 로고
    • ed. J. Vicens and V. Böhmer, Kluwer Academic Publishers, Dordrecht; values >90° mean that the phenolic unit is bent outwards
    • M. Perrin and D. Oehler in Calixarenes, A Versatile Class of Macrocyclic Compounds, ed. J. Vicens and V. Böhmer, Kluwer Academic Publishers, Dordrecht, 1991; values >90° mean that the phenolic unit is bent outwards.
    • (1991) Calixarenes, a Versatile Class of Macrocyclic Compounds
    • Perrin, M.1    Oehler, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.