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Volumn 44, Issue 23, 2003, Pages 4347-4350

The first stereoselective total synthesis of lankanolide. Part 2

Author keywords

[No Author keywords available]

Indexed keywords

ACID; LACTONE DERIVATIVE; LANKAMYCIN; LANKANOLIDE; UNCLASSIFIED DRUG;

EID: 0037693708     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)00955-9     Document Type: Article
Times cited : (9)

References (14)
  • 3
    • 0000751968 scopus 로고
    • In this case, the ratio of desired anti-Cram syn-adduct to undesired products was 6:1, although the structures of the undesired products were not determined
    • Keck, G. E.; Abott, D. E. Tetrahedron Lett. 1984, 25, 1883. In this case, the ratio of desired anti-Cram syn-adduct to undesired products was 6:1, although the structures of the undesired products were not determined.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 1883
    • Keck, G.E.1    Abott, D.E.2
  • 5
    • 0000416437 scopus 로고
    • and reference cited therein. In our case, the ratio of Cram to anti-Cram was 5:1, although only erythro-type adduct was obtained
    • Yamamoto, Y.; Yatagai, H.; Ishihara, Y.; Maeda, N.; Maruyama, K. Tetrahedron 1984, 40, 2239 and reference cited therein. In our case, the ratio of Cram to anti-Cram was 5:1, although only erythro-type adduct was obtained.
    • (1984) Tetrahedron , vol.40 , pp. 2239
    • Yamamoto, Y.1    Yatagai, H.2    Ishihara, Y.3    Maeda, N.4    Maruyama, K.5
  • 8
    • 85031166304 scopus 로고    scopus 로고
    • 1 bulkiness of the alcohol of seco-acid 3 may be the reason for the low yield, not because of disadvantageous conformational.
    • 1 bulkiness of the alcohol of seco-acid 3 may be the reason for the low yield, not because of disadvantageous conformational.
  • 13
    • 85031176491 scopus 로고    scopus 로고
    • 14 [α]=-27.8° (c 1.16, EtOH)
    • 14 [α]=-27.8° (c 1.16, EtOH).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.