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Volumn 73, Issue 11, 2008, Pages 4233-4236

Novel chiral calix[4]arenes by direct asymmetric epoxidation reaction

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CHEMICAL REACTIONS; EPOXIDATION;

EID: 44949161177     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800301m     Document Type: Article
Times cited : (24)

References (39)
  • 3
    • 0004268367 scopus 로고    scopus 로고
    • The Royal Society of Chemistry: Cambridge, UK
    • (c) Gutsche, C. D. Calixarenes Revisited; The Royal Society of Chemistry: Cambridge, UK, 1998.
    • (1998) Calixarenes Revisited
    • Gutsche, C.D.1
  • 4
    • 0004146786 scopus 로고
    • The Royal Society of Chemistry: Cambridge, UK
    • (d) Gutsche, C. D. Calixarenes; The Royal Society of Chemistry: Cambridge, UK, 1989.
    • (1989) Calixarenes
    • Gutsche, C.D.1
  • 23
    • 44949246819 scopus 로고    scopus 로고
    • On this subject we are also working on the preparation of suitable 1,3 calix[4]arenes, bearing commercially available and synthetic 1,2 amino alcohol subunits on the upper rim: Bonini, C.; Chiummiento, L.; Funicello, M.; Lopardo, M. T.; Lupattelli, P.; Velluzzi, E.; Viggiani, L. FIMOC IV Annecy (France) 2004, P14.
    • On this subject we are also working on the preparation of suitable 1,3 calix[4]arenes, bearing commercially available and synthetic 1,2 amino alcohol subunits on the upper rim: Bonini, C.; Chiummiento, L.; Funicello, M.; Lopardo, M. T.; Lupattelli, P.; Velluzzi, E.; Viggiani, L. FIMOC IV Annecy (France) 2004, P14.
  • 24
    • 44949235095 scopus 로고    scopus 로고
    • Bonini, C.; Lupattelli, P. ARKIVOC 2008, Part (viii), p 150.
    • Bonini, C.; Lupattelli, P. ARKIVOC 2008, Part (viii), p 150.
  • 32
    • 44949245880 scopus 로고    scopus 로고
    • 3) was used in the first dipropylation step, and the last exhaustive propylation was performed directly on the bis-aldehyde, obtaining the desired bis-aldehyde 1 in 60% overall yield from commercial calix[4]arene.
    • 3) was used in the first dipropylation step, and the last exhaustive propylation was performed directly on the bis-aldehyde, obtaining the desired bis-aldehyde 1 in 60% overall yield from commercial calix[4]arene.
  • 38
    • 44949119925 scopus 로고    scopus 로고
    • Sheldrick. G. M. SHELXL97, Programs for Crystal Structure Analysis (Release 97-2); University of Göttingen: Göttingen, Germany, 1997.
    • Sheldrick. G. M. SHELXL97, Programs for Crystal Structure Analysis (Release 97-2); University of Göttingen: Göttingen, Germany, 1997.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.