170937-60-7Relevant academic research and scientific papers
New Method for Derivatization of Squaric Acid to Highly Substituted Cyclobutenones: Lewis Acid-Catalyzed Reaction of Cyclobutene-1,2-dione Monoacetal and Its Vinylog with Unsaturated Organosilanes, and Subsequent Ring Transformation of the Adducts
Yamamoto, Yoshihiko,Ohno, Masatomi,Eguchi, Shoji
, p. 1353 - 1362 (1996)
Described herein is a novel method for regio-controlled synthesis of highly substituted cyclobutenones having an unsaturated substituent at 4-position, starting from commercially available squaric acid. Both cyclobutene-1,2-dione monoacetal (4,4-diethoxycyclobutenone) and its vinylog (2,4-diethoxycyclobutenone), which were easily obtained from diethyl squarate, reacted with allylsilanes in the presence of Et2O-BF3 to afford 4-allyl-4-ethoxycyclobutenones having various substituents at 2-position regioselectively. These products were efficiently transformed to highly substituted bicyclo[3.2.0]heptenones by refluxing in xylene. The synthetic utility of this process was demonstrated in the construction of tricyclic ring systems. Further extension of the Lewis acid-catalyzed reaction of the monoacetal using an allenylsilane, a silyl enol ether, and a silyl ketene acetal also afforded the corresponding 4-substituted products. In contrast to the above 4-allylated products, 4-propargylated and 4-acylmethylated products did not undergo an analogous ring transformation under the same conditions.
Radical-mediated ring enlargement of cyclobutenones: New synthetic potential of squaric acid
Yamamoto, Yoshihiko,Ohno, Masatomi,Eguchi, Shoji
, p. 9653 - 9661 (2007/10/02)
4-Hydroxy-2-cyclobutenones, which are readily obtainable from diethyl squarate, reacted with lead tetraacetate to give 5-acetoxy-2(5H)-furanones and 5-alkylidene-2(5H)-furanones via oxy-radical-triggered ring opening (β-scission) and subsequent 5-endo rec
