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Volumn 43, Issue 17, 2004, Pages 2293-2296

An efficient synthesis of lactacystin β-lactone

Author keywords

Aldol reaction; Heterocycles; Natural products; Reduction; Total synthesis

Indexed keywords

AMMONIA; CHEMICAL REACTIONS; ORGANIC COMPOUNDS;

EID: 4043159247     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200453843     Document Type: Article
Times cited : (68)

References (30)
  • 9
    • 0033583532 scopus 로고    scopus 로고
    • J. S. Panek, C. E. Masse, Angew. Chem. 1999, 111, 1161; Angew. Chem. Int. Ed. 1999, 38, 1093.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1093
  • 20
    • 0032479233 scopus 로고    scopus 로고
    • E. J. Corey, W. Li, T. Nagamitsu, Angew. Chem. 1998, 110, 1784; Angew. Chem. Int. Ed. 1998, 37, 1676.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1676
  • 27
    • 4544358690 scopus 로고    scopus 로고
    • note
    • X-ray crystal structure analysis was performed by Dr. A. Cowley, University of Oxford.
  • 28
    • 4544234396 scopus 로고    scopus 로고
    • note
    • 2CHLi all failed to displace the bromide.
  • 30
    • 4544268775 scopus 로고    scopus 로고
    • note
    • In compound 17, irradiation of 3-H led to an NOE enhancement of 4-H, but not of the methyl group at C4. In compound 18, irradiation of the 3-H led to NOE enhancements of both 4-H and of the methyl group at C4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.