期刊:Synlett [Thieme Medical Publishers (Germany)] 日期:2013-08-08卷期号:24 (15): 2014-2018被引量:10
标识
DOI:10.1055/s-0033-1338967
摘要
The Ugi reaction is a useful four-component coupling reaction for α-(acylamino)amide. However, selective transformation of the two amides is generally difficult. Here, we report 1-hydroxy-2-methyl-2-propyl isocyanide (HMPI) as a new member of a ‘convertible isocyanide’ class used to solve the problem. HMPI is odorless and shows good reactivity in the Ugi reaction to give N-(1-hydroxy-2-methyl-2-propyl) amides, which are smoothly converted into esters upon Zn(OTf)2-mediated solvolysis. Overall, structurally diverse α-amino acid esters are readily accessible in two steps by using HMPI.