메뉴 건너뛰기




Volumn 68, Issue 7, 2003, Pages 2760-2764

A short, stereocontrolled, and practical synthesis of α-methylomuralide, a potent inhibitor of proteasome function

Author keywords

[No Author keywords available]

Indexed keywords

STEREOCONTROL;

EID: 0037419155     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0268916     Document Type: Article
Times cited : (67)

References (37)
  • 14
    • 0032542772 scopus 로고    scopus 로고
    • Synthetic 1 and 2 are available from Calbiochem-Novabiochem Corp and Biomol Research Labs Inc.
    • Corey, E. J.; Li, W.; Reichard, G. A. J. Am. Chem. Soc. 1998, 120, 2330. Synthetic 1 and 2 are available from Calbiochem-Novabiochem Corp. and Biomol Research Labs, Inc.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 2330
    • Corey, E.J.1    Li, W.2    Reichard, G.A.3
  • 34
    • 0242558714 scopus 로고    scopus 로고
    • note
    • 2O or silica gel.
  • 36
    • 0242558715 scopus 로고    scopus 로고
    • note
    • 2. The face selectivity of coupling at the formyl center of 12 is readily explained in terms of a bidentate coordination of the formyl and methoxycarbonyl oxygens with lithium.
  • 37
    • 0242474983 scopus 로고    scopus 로고
    • note
    • Except for the labile aldehyde 12, all synthetic intermediates were readily purified by column chromatography on silica gel or by recrystallization (in the case of solids). Satisfactory spectroscopic and high-resolution mass spectral data were obtained for each reaction product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.