Advances in Metal-Mediated Solid-Phase Synthesis of Heterocyclic Compounds

Author(s):  
Agustina La-Venia ◽  
Carina M. L. Delpiccolo ◽  
Ernesto G. Mata
2003 ◽  
Vol 1 (11) ◽  
pp. 1909 ◽  
Author(s):  
Colin L. Gibson ◽  
Salvatore La Rosa ◽  
Colin J. Suckling

2001 ◽  
Vol 66 (7) ◽  
pp. 1078-1106 ◽  
Author(s):  
Viktor Krchňák ◽  
Jennifer Smith ◽  
Josef Vágner

The acid lability of electron-rich N-benzylanilines has been exploited in a linker for the traceless solid-phase synthesis of benzimidazoles, 2-aminobenzimidazoles, quinoxalinones and tetrahydroquinoxalines. The target compound precursors were assembled on a solid-phase support derivatized with either a benzylamine or a benzhydrylamine linker. Exposure to an acidic reagent caused cleavage of the C(benzyl)-N(aniline) bond, releasing the product with only a hydrogen atom on the descending nitrogen. The Encore technique for directed sorting on SynPhase Lanterns has been developed and applied to combinatorial synthesis of generic drug discovery libraries.


2009 ◽  
Vol 62 (3) ◽  
pp. 208 ◽  
Author(s):  
Mohammed Abid ◽  
Béla Török ◽  
Xudong Huang

Over the years, microwave-assisted organic synthesis (MAOS) became a commonly applied mainstream tool for the synthesis of heterocyclic compounds. The broad range of emerging applications in this field is mainly due to the significant contribution of MAOS to the development of ecofriendly processes. Various transformations have been developed for the synthesis of N-heterocycles under microwave conditions, including fast and selective processes. Tandem reactions involving greener reaction media, solvent-free conditions, and solid-phase synthesis are of exceptional interest in this area. In most transformations, microwave conditions dramatically enhanced reaction rates, as well as provided improved yields. This account highlights the most recent advancements in MAOS-based tandem processes for the synthesis of N-heterocycles.


2009 ◽  
Vol 62 (4) ◽  
pp. 392
Author(s):  
Mohammed Abid ◽  
Béla Török ◽  
Xudong Huang

Over the years, microwave-assisted organic synthesis (MAOS) became a commonly applied mainstream tool for the synthesis of heterocyclic compounds. The broad range of emerging applications in this field is mainly due to the significant contribution of MAOS to the development of ecofriendly processes. Various transformations have been developed for the synthesis of N-heterocycles under microwave conditions, including fast and selective processes. Tandem reactions involving greener reaction media, solvent-free conditions, and solid-phase synthesis are of exceptional interest in this area. In most transformations, microwave conditions dramatically enhanced reaction rates, as well as provided improved yields. This account highlights the most recent advancements in MAOS-based tandem processes for the synthesis of N-heterocycles.


1998 ◽  
Vol 56 (1) ◽  
pp. 2-10 ◽  
Author(s):  
Yoshinori KONDO ◽  
Hisashi SHINKAI ◽  
Ken-ichi TANJI

1997 ◽  
Vol 38 (6) ◽  
pp. 931-934 ◽  
Author(s):  
Adel Nefzi ◽  
John M. Ostresh ◽  
Jean-Philippe Meyer ◽  
Richard A. Houghten

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