TY - JOUR
T1 - Development of Chiral Ureates as Chiral Strong Brønsted Base Catalysts
AU - Kondoh, Azusa
AU - Ishikawa, Sho
AU - Terada, Masahiro
N1 - Funding Information:
This research was supported by a Grant-in-Aid for Scientific Research from the JSPS (No. 16H06354 to M.T. and No. 16K05680 to A.K.). A.K. and M.T. thank Toyota Physical and Chemical Research Institute for financial support.
Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/2/26
Y1 - 2020/2/26
N2 - Recently, chiral Brønsted bases having high basicity have emerged as a powerful tool in developing new catalytic enantioselective reactions. However, such chiral strong Brønsted base catalysts are still very scarce. Herein, we report the development of a chiral anionic Brønsted base having a N,N′-dialkyl ureate moiety as a basic site. Its prominent catalytic activity was demonstrated in the enantioselective addition reactions of α-thioacetamides as less acidic pronucleophiles with various electrophiles. Thus, the newly developed chiral catalyst with high accessibility and structural tunability would expand the scope of viable enantioselective transformations under Brønsted base catalysis.
AB - Recently, chiral Brønsted bases having high basicity have emerged as a powerful tool in developing new catalytic enantioselective reactions. However, such chiral strong Brønsted base catalysts are still very scarce. Herein, we report the development of a chiral anionic Brønsted base having a N,N′-dialkyl ureate moiety as a basic site. Its prominent catalytic activity was demonstrated in the enantioselective addition reactions of α-thioacetamides as less acidic pronucleophiles with various electrophiles. Thus, the newly developed chiral catalyst with high accessibility and structural tunability would expand the scope of viable enantioselective transformations under Brønsted base catalysis.
UR - http://www.scopus.com/inward/record.url?scp=85081013443&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85081013443&partnerID=8YFLogxK
U2 - 10.1021/jacs.9b13922
DO - 10.1021/jacs.9b13922
M3 - Article
C2 - 32043878
AN - SCOPUS:85081013443
SN - 0002-7863
VL - 142
SP - 3724
EP - 3728
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 8
ER -