메뉴 건너뛰기




Volumn 41, Issue 10, 2000, Pages 1559-1563

Total synthesis of macrosphelides B and A

Author keywords

Biologically active compounds; Macrolide; Macrosphelide A; Macrosphelide B; Oxidation of furans; Stereocontrol

Indexed keywords

FURAN DERIVATIVE; MACROLIDE; MACROSPHELIDE A; MACROSPHELIDE B; UNCLASSIFIED DRUG;

EID: 0034603460     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)02323-0     Document Type: Article
Times cited : (36)

References (28)
  • 4
    • 4243916088 scopus 로고    scopus 로고
    • (a) Omura, S.; Shiomi, K. Baiosaiensu to Indasutori 1996, 54, 633-635; Chem. Abstr. 1996, 125, 299445v.
    • (1996) Chem. Abstr. , vol.125
  • 6
    • 0031490120 scopus 로고    scopus 로고
    • (b) Ishizuka, M. Nippon Nogei Kagaku Kaishi, 1997, 71, 527-529; Chem. Abstr. 1997, 127, 12893x.
    • (1997) Chem. Abstr. , vol.127
  • 10
    • 0342354255 scopus 로고    scopus 로고
    • The enantiomeric purity of 85% ee inevitably results in a lower product-ratio of the desired stereoisomer vs the other isomers after joining the two parts, both of which were derived from the diol
    • The enantiomeric purity of 85% ee inevitably results in a lower product-ratio of the desired stereoisomer vs the other isomers after joining the two parts, both of which were derived from the diol.
  • 17
    • 0342789207 scopus 로고    scopus 로고
    • 1H NMR spectroscopy of the derived MTPA ester
    • 1H NMR spectroscopy of the derived MTPA ester.
  • 22
    • 0343223758 scopus 로고    scopus 로고
    • 2SiCl, imidazole, DMF) followed by hydrolysis (1N NaOH, MeOH) in 91% yield
    • 2SiCl, imidazole, DMF) followed by hydrolysis (1N NaOH, MeOH) in 91% yield.
  • 27
    • 0342354250 scopus 로고    scopus 로고
    • 9: C, 56.24; H, 6.29. Found: C, 55.99; H, 6.23
    • 9: C, 56.24; H, 6.29. Found: C, 55.99; H, 6.23.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.