First total synthesis of (±)-kenusanone b

Article abstract of DOI:10.1080/00397919808004863

The first total synthesis of a natural prenylflavanone, (±)-kenusanone B (1) has been achieved by condensation of acetophenone 4 and benzaldehyde 6 followed by cyclization and deprotection. Chloromethyl methyl ether was used as a facile protecting reagent of free hydroxy groups for the synthesis of polyhydroxylated flavanones.

Full text of DOI:10.1080/00397919808004863

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Synthetic Communications:
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First Total Synthesis of (±)-
Kenusanone B
Li Xiao a , Wenfei Tan a & Yulin Li a
a National Laboratory of Applied Organic
Chemistry and Institue of Organic Chemistry,
Lanzhou University , Lanzhou, 730000, P. R.
China
Published online: 20 Aug 2006.
To cite this article: Li Xiao , Wenfei Tan & Yulin Li (1998) First Total Synthesis
of (±)-Kenusanone B, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 28:15, 2861-2869, DOI:
10.1080/00397919808004863
To link to this article: http://dx.doi.org/10.1080/00397919808004863
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