Gold-catalyzed tandem cycloisomerization/Petasis–Ferrier rearrangement: a direct route to 3-alkoxyindanones from enynals and alcohols
A method to prepare 3-alkoxyindanones by gold-catalyzed tandem cycloisomerization/Petasis–Ferrier rearrangement of ortho-ethynylarylaldehydes with alcohols is described. The reaction also offers a synthetic route to 3-alkoxylcyclopentenones.
2014 ◽
Vol 4
(31)
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pp. 10-14
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2019 ◽
Vol 19
(17)
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pp. 1392-1406
2019 ◽
Vol 16
(6)
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pp. 447-453
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Keyword(s):