Organocatalytic 1,4‐Addition Reaction of 2‐Formyl(thio)esters to Vinylketones: An Efficient Access to Acyclic Chiral Building Blocks with a Quaternary Carbon Stereocenter |
| |
| Authors: | Toshifumi Tatsumi Dr. Tomonori Misaki Prof. Dr. Takashi Sugimura |
| |
| Affiliation: | Graduate School of Material Science, University of Hyogo, 3‐2‐1 Kohto, Kamigori, Hyogo 678‐1297 (Japan) |
| |
| Abstract: | 2‐Formyl(thio)esters were utilized as pronucleophiles to obtain less‐accessible acyclic chiral building blocks bearing versatile functional groups on a quaternary carbon atom for enantioselective 1,4‐addition to vinylketones. To achieve high enantioselectivity in the present 1,4‐addition reaction, thiourea‐tertiary amines containing a bulky chiral backbone were developed as catalysts, and several derivatizations of the products were performed to demonstrate the synthetic utility of the products. |
| |
| Keywords: | aldehydes asymmetric catalysis enones Michael addition organocatalysis |
|
|
