
Journal of Organic Chemistry p. 2029 - 2033 (1987)
Update date:2022-07-30
Topics: Total synthesis Chemical Synthesis Starting Materials Natural product Experimental conditions therapeutic properties Organic Molecule
Shih, Thomas L.
Wyvratt, Matthew J.
Mrozik, Helmut
A novel intramolecular Mitsunobu alkylation is employed to construct the benzopyran moiety of the newly isolated isoflavan 5-O-methyllicoricidin.This convergent 15-step total synthesis outlines a chemically mild approach to the acid-sensitive isoflavanoid
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Doi:10.1007/BF00765114
(1987)Doi:10.1016/S0040-4039(01)93475-6
(1989)Doi:10.1002/jhet.5570230426
(1986)Doi:10.1246/cl.1986.2109
(1986)Doi:10.1016/j.tetlet.2009.09.085
(2009)Doi:10.1021/jo00292a040
(1990)