TY  - JOUR
ID  - pittir19097
UR  - http://d-scholarship-dev.library.pitt.edu/19097/
IS  - 9
A1  - Zhang, W
A1  - Lu, Y
A1  - Chen, CHT
A1  - Curran, DP
A1  - Geib, S
Y1  - 2006/04/28/
N2  - Fluorous proline derivatives generated from one-pot, three-component [3+2] cycloaddition of azomethine ylides are employed in different post-condensation reactions to form hydantoin-, piperazinedione-, and benzodiazepinedione-fused tricyclic and tetracyclic ring systems. High synthetic efficiency is achieved by conducting fast microwave reactions and purification by easy fluorous solid-phase extractions. Methods developed for these novel drug-like heterocyclic compounds can be applied to diversity-oriented library syntheses. © Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
JF  - European Journal of Organic Chemistry
SN  - 1434-193X
TI  - Fluorous synthesis of hydantoin-, piperazinedione-, and benzodiazepinedione-fused tricyclic and tetracyclic ring systems
SP  - 2055 
AV  - public
EP  -  2059
ER  -