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Volumn 20, Issue 4, 2008, Pages 397-405

Mini-review: Artificial catecholamine receptors in aqueous media

Author keywords

Catecholamine; Molecular recognition; Receptor design; Selectivity; Water

Indexed keywords


EID: 42949103484     PISSN: 10610278     EISSN: 10290478     Source Type: Journal    
DOI: 10.1080/10610270701278269     Document Type: Article
Times cited : (17)

References (30)
  • 5
    • 42949110379 scopus 로고    scopus 로고
    • An RNA-aptamer derived from in vitro selection experiments is also discussed here, but the lack of structural information defies categorizing, despite functional similarities
    • An RNA-aptamer derived from in vitro selection experiments is also discussed here, but the lack of structural information defies categorizing, despite functional similarities.
  • 6
    • 42949101523 scopus 로고    scopus 로고
    • Schneider, H.-J.; Yatsimirsky, A. K. Principles and Methods in Supramolecular Chemistry; John Wiley: New York, 2000; p xii, 349.
    • Schneider, H.-J.; Yatsimirsky, A. K. Principles and Methods in Supramolecular Chemistry; John Wiley: New York, 2000; p xii, 349.
  • 27
    • 10744231349 scopus 로고    scopus 로고
    • See Molt, O.; Rubeling, D.; Schrader, G. J. Am. Chem. Soc. 2003, 125, 12086. (Similar concept has been advanced by Schrader's group, using a structure similar to that of a ring-opened 18. While the tweezer structures were reported to be active in MeOH, no activity in water was shown, presumably due to inactivity. The difference is likely due to the incomplete preorganization in the tweezer structures, where a benzyl bond is allowed to freely rotate).
    • See Molt, O.; Rubeling, D.; Schrader, G. J. Am. Chem. Soc. 2003, 125, 12086. (Similar concept has been advanced by Schrader's group, using a structure similar to that of a ring-opened 18. While the tweezer structures were reported to be active in MeOH, no activity in water was shown, presumably due to inactivity. The difference is likely due to the incomplete preorganization in the tweezer structures, where a benzyl bond is allowed to freely rotate).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.