One-pot synthesis of pyrrolo[1,2-a]quinoxaline and pyrrolo[1,2-a]pyrazine derivatives via the three-component reaction of 1,2-diamines, ethyl pyruvate and α-bromo ketones
暂无分享,去创建一个
[1] L. Moradi,et al. One-pot multicomponent synthesis of novel tricyclic pyrrolo[2,1-c][1,4]benzoxazines , 2014 .
[2] L. Moradi,et al. One-pot synthesis of pyrrolo[1,2-a]pyrazines via three component reaction of ethylenediamine, acetylenic esters and nitrostyrene derivatives , 2013 .
[3] L. Moradi,et al. A one-pot catalyst-free synthesis of functionalized pyrrolo[1,2-a]quinoxaline derivatives from benzene-1,2-diamine, acetylenedicarboxylates and ethyl bromopyruvate , 2013, Beilstein journal of organic chemistry.
[4] A. Furlan,et al. 'Click' synthesis of a triazole-based inhibitor of Met functions in cancer cells. , 2012, Bioorganic & medicinal chemistry letters.
[5] Vipender Singh,et al. AuI-Catalyzed Direct Hydroamination/Hydroarylation and Double Hydroamination of Terminal Alkynes , 2010 .
[6] N. T. Patil,et al. Platinum-catalyzed formal Markownikoff's hydroamination/hydroarylation cascade of terminal alkynes assisted by tethered hydroxyl groups. , 2009, The Journal of organic chemistry.
[7] I. Yavari,et al. Synthesis of pyrrolo[2,1-a]isoquinolines from activated acetylenes, benzoylnitromethanes, and isoquinoline , 2009 .
[8] C. Bolm,et al. Iron-catalysed carbon-heteroatom and heteroatom-heteroatom bond forming processes. , 2008, Chemical Society reviews.
[9] Rob Leurs,et al. Fragment based design of new H4 receptor-ligands with anti-inflammatory properties in vivo. , 2008, Journal of medicinal chemistry.
[10] Chae S. Yi,et al. Scope and mechanistic study of the ruthenium-catalyzed ortho-C-H bond activation and cyclization reactions of arylamines with terminal alkynes. , 2005, Journal of the American Chemical Society.
[11] N. Monteiro,et al. Pd‐Assisted Multicomponent Synthesis of Heterocycles , 2003 .
[12] L. Weber. Multi-component reactions and evolutionary chemistry. , 2002, Drug discovery today.
[13] B. Insuasty,et al. A versatile synthesis of 4,5‐dihydropyrrolo[1,2‐a]quinoxalines , 2001 .
[14] R. David,et al. Changing therapeutic paradigms in glaucoma management. , 1998, Expert opinion on investigational drugs.
[15] G. Adams,et al. Heterocyclic mono-N-oxides with potential applications as bioreductive anti-tumour drugs: Part 1. 8-Alkylamino-substituted phenylimidazo [1,2-a] quinoxalines. , 1993, Anti-cancer drug design.
[16] A. Furlan,et al. Identification of new aminoacid amides containing the imidazo[2,1-b]benzothiazol-2-ylphenyl moiety as inhibitors of tumorigenesis by oncogenic Met signaling. , 2012, European journal of medicinal chemistry.