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Volumn 46, Issue 9, 2005, Pages 1529-1532

Cu-catalysed asymmetric 1,4-addition of Me3Al to nitroalkenes. Synthesis of (+)-ibuprofen

Author keywords

Aluminium; Asymmetry; Conjugate addition; Copper; Ibuprofen; Nitro

Indexed keywords

ALKENE; ALUMINUM DERIVATIVE; COPPER DERIVATIVE; COPPER THIOPHENECARBOXYLIC ACID; IBUPROFEN; PHOSPHORAMIDIC ACID; UNCLASSIFIED DRUG;

EID: 13444269426     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.01.007     Document Type: Article
Times cited : (57)

References (38)
  • 9
    • 13444260537 scopus 로고    scopus 로고
    • Methodologies in Asymmetric Catalysis, Malhotra, S. V., Ed. Washington Chapter 4
    • Alexakis, A. In Methodologies in Asymmetric Catalysis, Malhotra, S. V., Ed. ACS Symposium Series 880; Washington, 2004; Chapter 4, pp 43-59
    • (2004) ACS Symposium Series 880 , pp. 43-59
    • Alexakis, A.1
  • 10
    • 0034975355 scopus 로고    scopus 로고
    • For Rh-catalysed 1,4-addition of aryl boronates onto nitroalkenes, see: T. Hayashi Synlett 2001 879 887
    • (2001) Synlett , pp. 879-887
    • Hayashi, T.1
  • 38
    • 0141630613 scopus 로고    scopus 로고
    • note
    • 3) for 97.2% ee (Harrington-Frost, N.; Leuser, H.; Calaza, M. I.; Kneisel, F. F.; Knochel, P. Org. Lett. 2003, 5, 2111-2114). Ee was measured by chiral SFC (Chiralcel OJ column, 5% MeOH during 2 min, then 1%/min 2 mL/min): R-(-) enantiomer: 3.31′. S-(+) enantiomer: 3.60′


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.