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