Catalytic enantioselective Michael addition of 1,3-dicarbonyl compounds to nitroalkenes catalyzed by well-defined chiral ru amido complexes

Journal of the American Chemical Society
Masahito WatanabeTakao Ikariya

Abstract

Well-defined chiral Ru amido complexes promoted asymmetric Michael addition of 1,3-dicarbonyl compounds including malonates, beta-keto esters, and 1,3-diketones to nitroalkenes to give the corresponding adducts with excellent ees and in excellent yields.

Citations

Oct 30, 2010·Journal of the American Chemical Society·Ilya D GridnevTakao Ikariya
Mar 14, 2009·Journal of the American Chemical Society·Barry M Trost, Julien Hitce
Dec 18, 2013·The Journal of Organic Chemistry·Daniel Best, Hon Wai Lam
May 11, 2013·Organic Letters·Alain J Simpson, Hon Wai Lam
Mar 12, 2010·Dalton Transactions : an International Journal of Inorganic Chemistry·Shigeki Kuwata, Takao Ikariya
Aug 19, 2010·Chemical Communications : Chem Comm·Takahiro NishimuraTamio Hayashi
Mar 25, 2011·Chemical Communications : Chem Comm·Kilian MuñizMarta Martínez Belmonte
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Feb 1, 2006·Organic & Biomolecular Chemistry·Takao IkariyaRyoji Noyori
Jan 30, 2010·Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry·Makoto FurutachiMasakatsu Shibasaki
Jan 27, 2007·Chemistry : a European Journal·Celia M MayaAngeles Monge
Mar 24, 2009·Chemical Record : an Official Publication of the Chemical Society of Japan ... [et Al.]·Takao Ikariya, Ilya D Gridnev
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