%0 Journal Article %A Zhang, Liming %A Koreeda, Masato %D 2002 %T Stereocontrolled Synthesis of Kelsoene by the Homo-Favorskii Rearrangement %U https://acs.figshare.com/articles/journal_contribution/Stereocontrolled_Synthesis_of_Kelsoene_by_the_Homo-Favorskii_Rearrangement/3744264 %R 10.1021/ol026739q.s001 %2 https://ndownloader.figshare.com/files/5837625 %K 16 steps %K Ketone 15 %K isomerized %K enolate %K intramolecular S N 2 product 15 %K Kelsoene %K acid treatment %K Stereocontrolled Synthesis %K cyclobutanone 17 %K tosylate %K Rearrangement %K dihydroanisole %K keto %K kelsoene carbon skeleton %K rearrangement %X (±)-Kelsoene (4) has been synthesized from 2,5-dihydroanisole in 16 steps in 12.5% overall yield. The key step involves a base-catalyzed reaction of γ-keto tosylate (5), which effects a homo-Favorskii rearrangement to 16 as well as the corresponding intramolecular SN2 product 15 from the enolate of 5. Ketone 15 can efficiently be isomerized to cyclobutanone 17 having the kelsoene carbon skeleton upon acid treatment. %I ACS Publications