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Volumn , Issue 22, 2003, Pages 4422-4431

The Reductive Fragmentation of 7-Hydroxy-9,10-dioxotaxoids

Author keywords

Antitumour agents; Natural products; Taxoids; Terpenoids

Indexed keywords

ALUMINUM DERIVATIVE; ANTINEOPLASTIC AGENT; CERIUM; SOLVENT; TAXANE DERIVATIVE; TAXOID;

EID: 0344845008     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300376     Document Type: Article
Times cited : (9)

References (35)
  • 33
    • 0028216840 scopus 로고
    • The stability of the lactone ring of 18 towards hydrides is not surprising, since functional groups protruding from the taxane skeleton can have a low reactivity, as observed for the primary hydroxy group of 19-hydroxy-10-deacetylbaccatin III: R. Margraff, D. Bézard, J. D. Bourzat, A. Commerçon, Bioorg. Med. Chem. Lett. 1994, 4, 233-236..
    • (1994) Bioorg. Med. Chem. Lett. , vol.4 , pp. 233-236
    • Margraff, R.1    Bézard, D.2    Bourzat, J.D.3    Commerçon, A.4
  • 34
    • 0031833570 scopus 로고    scopus 로고
    • A remarkable example of a hydride-induced non-reductive transformation of a taxoid is the borohydride mediated anti-Michael hydration of the enone system of taxinine, a reaction presumably proceeding through the formation of a boron enolate, which undergoes autoxidation during workup: H. Suzuki, M. Sako, K. Hirota, Chem. Pharm. Bull. 1998, 46, 857-859.
    • (1998) Chem. Pharm. Bull. , vol.46 , pp. 857-859
    • Suzuki, H.1    Sako, M.2    Hirota, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.