TY - JOUR
T1 - 7α-Alkoxyestra-1,3,5(10)-trienes
AU - Yasuda, Takumi
AU - Shima, Yuji
AU - Ideta, Keiko
AU - Das Neves Oliveira, Cristina
AU - Thiemann, Thies
PY - 2008/1
Y1 - 2008/1
N2 - α-Alkoxyestradiols were prepared through LiAlH4 reduction of a suitably protected 6α,7α-epoxyestra-1,3,5(10)-trien-3-ol-17- one, alkylation of the resultant 7α-hydroxyestra-1,3,5(10)-trien-3-ol-17- one derivative and subsequent transformation of the C17 functionality.
AB - α-Alkoxyestradiols were prepared through LiAlH4 reduction of a suitably protected 6α,7α-epoxyestra-1,3,5(10)-trien-3-ol-17- one, alkylation of the resultant 7α-hydroxyestra-1,3,5(10)-trien-3-ol-17- one derivative and subsequent transformation of the C17 functionality.
KW - Estradiol
KW - Ethers
KW - Steroids
UR - http://www.scopus.com/inward/record.url?scp=42349097797&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=42349097797&partnerID=8YFLogxK
U2 - 10.3184/030823408X287140
DO - 10.3184/030823408X287140
M3 - Article
AN - SCOPUS:42349097797
SN - 0308-2342
SP - 32
EP - 37
JO - Journal of Chemical Research
JF - Journal of Chemical Research
IS - 1
ER -