1037681-49-4Relevant articles and documents
Facile carbamoylation of 3,4-dihydropyridin-2-one with N-chlorosulfonyl isocyanate
Sa?ański, Piotr,Young, Kwan Ko,Lee, Kee-In
, p. 46 - 48 (2006)
3,4-Dihydro-2-pyridone-5-carboxylic acid amides were prepared by carbamoylation at the C-5 position of 3,4-dihydropyridin-2-one with N-chlorosulfonyl isocyanate.
Synthesis of Cyclic Imides by Acceptorless Dehydrogenative Coupling of Diols and Amines Catalyzed by a Manganese Pincer Complex
Espinosa-Jalapa, Noel Angel,Kumar, Amit,Leitus, Gregory,Diskin-Posner, Yael,Milstein, David
supporting information, p. 11722 - 11725 (2017/09/07)
The first example of base-metal-catalyzed dehydrogenative coupling of diols and amines to form cyclic imides is reported. The reaction is catalyzed by a pincer complex of the earth abundant manganese and forms hydrogen gas as the sole byproduct, making the overall process atom economical and environmentally benign.
Direct site-selective arylation of enamides via a decarboxylative cross-coupling reaction
Gigant, Nicolas,Chausset-Boissarie, La?titia,Gillaizeau, Isabelle
supporting information, p. 816 - 819 (2013/03/28)
An efficient Pd-catalyzed decarboxylative cross-coupling reaction of simple enamides was achieved. Depending on the choice of the nitrogen-protecting group, a site-selective synthesis of mono- or diarylated framework(s) was performed under mild conditions
