Bulman Page, Philip C., McKenzie, Michael J. and Gallagher, James A. (2001) Novel synthesis of bis(phosphonic acid)-steroid conjugates. Journal of Organic Chemistry, 66 (11). pp. 3704-3708. ISSN 0022-3263
Full text not available from this repository.Abstract
An efficient synthesis has been realized for several members of a new class of potential bone resorption inhibitors consisting of steroidal oestrogenic units linked at the 3 and 17 positions to a geminal bisphosphonate moiety through an ester linkage of variable length. The convergent synthesis utilizes benzyl bisphosphonates, transesterification, and Meldrum's acid chemistry and has the potential to allow many oestrogenic derivatives as well as other biologically active compounds to be coupled to the geminal bisphosphonate moeity.
Item Type: | Article |
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Uncontrolled Keywords: | bone,osteoporosis,alendronate,analogs,estrogen,ovariectomized rats,bisphosphonates,postmenopausal women,resorption,mechanisms |
Faculty \ School: | Faculty of Science > School of Chemistry (former - to 2024) |
UEA Research Groups: | Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Materials and Catalysis |
Depositing User: | Rachel Smith |
Date Deposited: | 21 Jun 2011 11:19 |
Last Modified: | 24 Sep 2024 10:22 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/32827 |
DOI: | 10.1021/jo001489h |
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