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Enantioselective Synthesis of a Highly Substituted Tetrahyd..:
Maddess, Matthew L.
;
Scott, Jeremy P.
;
Alorati, Anthony
...
Organic Process Research & Development. 18 (2014) 4 - p. 528-538 , 2014
Link:
https://doi.org/10.1021/op5000489
RT Journal T1
Enantioselective Synthesis of a Highly Substituted Tetrahydrofluorene Derivative as a Potent and Selective Estrogen Receptor Beta Agonist
UL https://suche.suub.uni-bremen.de/peid=cr-10.1021_op5000489&Exemplar=1&LAN=DE A1 Maddess, Matthew L. A1 Scott, Jeremy P. A1 Alorati, Anthony A1 Baxter, Carl A1 Bremeyer, Nadine A1 Brewer, Sarah A1 Campos, Kevin A1 Cleator, Ed A1 Dieguez-Vazquez, Alejandro A1 Gibb, Andrew A1 Gibson, Andrew A1 Howard, Melissa A1 Keen, Stephen A1 Klapars, Artis A1 Lee, Jaemoon A1 Li, Jing A1 Lynch, Joseph A1 Mullens, Peter A1 Wallace, Debra A1 Wilson, Robert PB American Chemical Society (ACS) YR 2014 SN 1083-6160 SN 1520-586X JF Organic Process Research & Development VO 18 IS 4 SP 528 OP 538 LK http://dx.doi.org/https://doi.org/10.1021/op5000489 DO https://doi.org/10.1021/op5000489 SF ELIB - SuUB Bremen
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