111160-44-2Relevant articles and documents
Enantioselective copper(I/II)-catalyzed conjugate addition of nitro esters to β,γ-unsaturated α-ketoesters
Zhang, Sheng,Xu, Kun,Guo, Fengfeng,Hu, Yanbin,Zha, Zhenggen,Wang, Zhiyong
, p. 979 - 982 (2014/02/14)
A highly enantioselective Michael addition of nitroacetates to β,γ-unsaturated α-ketoesters was developed by using chiral copper catalysts. The Michael addition products can be obtained in high yields with up to 99 % ee. With these densely functionalized products, the chiral cyclic nitrones, which are important synthetic intermediates, can be obtained in one step. Copyright
Synthesis of α-Keto Esters via Palladium-Catalyzed Double Carbonylation
Sakakura, Toshiyasu,Yamashita, Hiroshi,Kobayashi, Toshi-aki,Hayashi, Teruyuki,Tanaka, Masato
, p. 5733 - 5740 (2007/10/02)
-