Synthesis p. 275 - 277 (1991)
Update date:2022-09-26
Topics:
Peterson
Do
Rogers
A four-step synthesis of the Bristol-Myers' precursor, ethyl rel-(3R,4R)-6,7-methylenedioxy-1-oxo-4-(3,4,5-trimethoxyphenyl)-1,2,3 ,4-tetrahydronaphthalene-3-carboxylate, to (±)-podophyllotoxin is described in 40% overall yield from ethyl 3,4,5-trimethoxy
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Doi:10.1002/chem.201300150
(2013)Doi:10.1002/chem.200900681
(2009)Doi:10.1016/j.tet.2018.11.007
(2018)Doi:10.1016/j.bmcl.2009.06.107
(2009)Doi:10.1021/ja01552a046
(1958)Doi:10.1021/jm901280q
(2009)
