Author:
Bull J.R.,Hodgkinson A.J.,Tuinman A.
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Cited by
7 articles.
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1. Quantitative electronic structure-activity relationship (QESAR) of natural cytotoxic compounds: maytansinoids, quassinoids and cucurbitacins;European Journal of Pharmaceutical Sciences;1994-12
2. Steroidal analogues of unnatural configuration. Part 14. Conformational analysis of 4,4,14α-trimethyl-19(10→9β)abeo-5β,10α-pregnane-6,11-diols by X-ray crystallography and force-field calculations;J. Chem. Soc., Perkin Trans. 2;1979
3. Steroidal analogues of unnatural configuration. Part 13. Synthesis and ringBreactions of 4,4,9-trimethyl-9β,10α-estr-5-ene;J. Chem. Soc., Perkin Trans. 1;1978
4. Steroidal analogues of unnatural configuration. Part 12. RingAreactions of 9-methyl-5β,9β,10α- and 9-methyl-5α,9β,10α-estran-3-ones: conformational analysis and X-ray crystallography of products;J. Chem. Soc., Perkin Trans. 1;1978
5. Steroidal analogues of unnatural configuration. Part XI. Crystal and molecular structure of 3α,17α-dihydroxy-4,4,14α-trimethyl-19-nor-10α-pregn-5-ene-11,20-dione and a circular dichroism study of the conformation of the acetyl side-chain of the 17-hydroxy-isomers in solution;J. Chem. Soc., Perkin Trans. 2;1977