Hydrogen-bond-mediated cascade reaction involving chalcones: facile synthesis of enantioenriched trisubstituted tetrahydrothiophenes.
Jun-Bing Ling, Yu Su, Hai-Liang Zhu, Guan-Yu Wang, Peng-Fei Xu
Index: Org. Lett. 14(4) , 1090-3, (2012)
Full Text: HTML
Abstract
A bifunctional squaramide catalyzed sulfa-Michael/aldol cascade reaction between 1,4-dithiane-2,5-diol and chalcones with a low catalyst loading has been developed. Trisubstituted tetrahydrothiophenes with three contiguous stereogenic centers are obtained in a highly stereocontrolled manner. Additionally, a remarkable temperature effect on reaction efficiency was observed and a synthetically potential gram-synthesis was also conducted.
Related Compounds
Related Articles:
2002-02-27
[J. Agric. Food Chem. 50(5) , 1126-32, (2002)]
1990-01-01
[Chem. Pharm. Bull. 38(1) , 243-5, (1990)]
2001-05-01
[Bioorg. Med. Chem. 9(5) , 1123-32, (2001)]
2013-11-01
[Org. Lett. 15(21) , 5554-7, (2013)]
1, 4-Dithiane-2, 5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes. Baricordi N, et al.
[Tetrahedron 68(1) , 208-213, (2012)]