Rubenbauer Philipp, Bach Thorsten
Lehrstuhl für Organische Chemie 1, Technische Universität München, 85747 Garching, Germany.
Chem Commun (Camb). 2009 Apr 28(16):2130-2. doi: 10.1039/b901937e. Epub 2009 Mar 17.
An acid-catalysed Ritter reaction of chiral secondary benzylic alcohols enables diastereoselective access to chiral amides, which represent inter alia valuable intermediates for the synthesis of chiral 1,2-diamines and beta-amino acids.
手性仲苄醇的酸催化 Ritter 反应能够非对映选择性地得到手性酰胺,这些手性酰胺尤其代表了用于合成手性 1,2 - 二胺和β - 氨基酸的有价值的中间体。