Diastereoselective Synthesis of Functionalized Diketopiperazines through Post-transformational Reactions Saeed Balalaie Reihaneh Ramezani Kejani Elmira Ghabraie Fatemeh Darvish Frank Rominger Fatima Hamdan Hamid Reza Bijanzadeh 10.1021/acs.joc.7b01855.s003 https://acs.figshare.com/articles/dataset/Diastereoselective_Synthesis_of_Functionalized_Diketopiperazines_through_Post-transformational_Reactions/5573818 A diversity-oriented access to diastereoselective arylidene 2,5-diketopiperazines is elaborated via a sequential Ugi post-transformation involving catalytic cyclization and oxidative Heck reaction sequence. This sequence offers an interesting multicomponent entry to a library of 2,5-diketopiperazines and arylidene 2,5-diketopiperazines under mild reaction conditions in good to excellent yields. 2017-10-19 00:00:00 arylidene multicomponent entry oxidative Heck reaction sequence sequential Ugi post-transformation reaction conditions diversity-oriented access Diastereoselective Synthesis Functionalized Diketopiperazines Post-transformational Reactions diketopiperazine