메뉴 건너뛰기




Volumn , Issue 9, 2001, Pages 1761-1768

Semisynthesis of flexible 5,7-dideoxypaclitaxel derivatives from Taxine B

Author keywords

Antitumor agents; Natural products; Structure activity relationships; Synthesis design; Taxine B

Indexed keywords

5,7 DIDEOXYPACLITAXEL; TAXANE DERIVATIVE; TAXOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0035042793     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200105)2001:9<1761::AID-EJOC1761>3.0.CO;2-O     Document Type: Article
Times cited : (7)

References (23)
  • 1
    • 0005050933 scopus 로고    scopus 로고
    • http://www.fda.gov/oashi/cancer/cdrug.html
  • 20
    • 0030484915 scopus 로고    scopus 로고
    • Formally, the preparation of 21 from methyl (E)-cinnamate can be shortened to 5 steps by carrying out a Sharpless asymmetric aminohydroxylation: G. Li, H. H. Angert, K. B. Sharpless, Angew. Chem. Int. Ed. Engl. 1996, 35, 2813-2817.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 2813-2817
    • Li, G.1    Angert, H.H.2    Sharpless, K.B.3
  • 22
    • 0005100824 scopus 로고    scopus 로고
    • note
    • The coupling of 28 to 27 proceeds with a slightly better yield than the coupling of 21 to 27, which makes it the method of choice.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.