170117-99-4Relevant articles and documents
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 (2007/10/03)
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.
BF3-Catalyzed Reaction of Cyclobutene-1,2-dione Monoacetal and Its Vinylog with Allylsilanes. Regioselective Synthesis of 4-Allyl-4-ethoxycyclobutenones from Squaric Acid and Their Conversion to Bi-and Tricycloalkanones
Yamamoto, Yoshihiko,Ohno, Masatomi,Eguchi, Shoji
, p. 525 - 526 (2007/10/03)
Regioselective allylation of 2,4- and 4,4-diethoxycyclobuteones was performed with allylsilanes in the presence of BF3*Et2O via a common ethoxycarbenium ion intermediate.A merit of this reaction was demonstrated in an efficient conversion of the obtained
