A Two-Step Synthesis of α-Keto Vinyl Carbinols from Ketones
Author:
Affiliation:
1. Laboratoire de Synthèse Organique, CNRS UMR 7652 Ecole Polytechnique, 91128 Palaiseau Cedex, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol4029594
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3. Acid-promoted reaction of cyclic allylic diols with carbonyl compounds. Stereoselective ring-enlarging tetrahydrofuran annulations
4. Pyrrole annulation onto aldehydes and ketones via palladium-catalyzed reactions
5. Acid-catalyzed ring expansion of 1-(1-methoxy-1,2-propadienyl)-2-cyclobuten-1-ols. Synthesis of 5-hydroxy-5-vinyl-2-cyclopenten-1-ones and their stereoselective transformation to 5-(2-acetoxyethylidene)-2-cyclopenten-1-ones
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