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Volumn 17, Issue 3, 2007, Pages 780-783

Synthesis and antiproliferative activity of (2R,3R)-disubstituted tetrahydropyrans. Part 2: Effect of side chain homologation

Author keywords

Anticancer drugs; Cyclic ethers; Marine products; Solid tumors; Structure activity relationship

Indexed keywords

TETRAHYDROPYRAN DERIVATIVE;

EID: 33846214455     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2006.10.066     Document Type: Article
Times cited : (11)

References (29)
  • 25
    • 33846225552 scopus 로고    scopus 로고
    • note
    • The orientation of the phenyl group was confirmed by NOE experiments. The stereochemical control in this reaction is a consequence of the formation of the most stable cis-decaline, which has the phenyl group on an equatorial orientation.
  • 28
    • 16244386216 scopus 로고    scopus 로고
    • ® appeared the most accurate predictor of Clog P values
    • ® appeared the most accurate predictor of Clog P values. Machatha S.G., and Yalkowsky S.H. Int. J. Pharm. 294 (2005) 185
    • (2005) Int. J. Pharm. , vol.294 , pp. 185
    • Machatha, S.G.1    Yalkowsky, S.H.2
  • 29
    • 33846227006 scopus 로고    scopus 로고
    • note
    • ® accessible via Internet (www.daylight.com/daycgi/clogp) working with the Hansch-Leo's 'fragment constant' method.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.