A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Product Details of 101187-40-0, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 101187-40-0, Name is tert-Butyl (2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)carbamate, molecular formula is C13H28N2O5. In an article, author is Ghiazza, Clement,once mentioned of 101187-40-0.
The C-C coupling reaction of N-electron withdrawing group (EWG) protected amides with coupling partners is one of the most important methods for C-C bond formation at the a-position of amides to directly give a-substituted amides. Of the four reactions, namely, the reaction via the generation of carbanion with an electrophile, that via the generation of carbon radical with a radical donor, that via the generation of iminium ion species with a nucleophile (oxidative coupling reaction), and that using a transition metal carbenoid, the oxidative coupling reaction presents a challenge although the reaction products are very useful for the transformation of a wide range of nitrogen-containing derivatives. In this review, recent developments in the oxidative coupling reaction of N-EWG protected amides with nucleophiles are summarized with focus on the reaction using a transition metal, the transition-metal-free reaction, the enantioselective reaction using a chiral catalysts, and the organocatalyzed oxidative coupling reaction. (C) 2017 Elsevier Ltd. All rights reserved.
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Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics