Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Frederic Lieby-Muller"'
Publikováno v:
European Journal of Organic Chemistry. 2013:4131-4145
A metal-free and completely regioselective three-component synthesis of highly functionalized pyridines from 1,3-dicarbonyl derivatives and Michael acceptors has been achieved. Activated Michael acceptors, that is, β,γ-unsaturated α-oxo carbonyl d
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2012, 354, pp.2537-2544. ⟨10.1002/adsc.201200412⟩
Advanced Synthesis and Catalysis, 2012, 354, pp.2537-2544. ⟨10.1002/adsc.201200412⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2012, 354, pp.2537-2544. ⟨10.1002/adsc.201200412⟩
Advanced Synthesis and Catalysis, 2012, 354, pp.2537-2544. ⟨10.1002/adsc.201200412⟩
International audience; We designed a new, user-friendly oxidative dual heterogeneous catalytic system capable of promoting polysubstituted pyridines as unique products from simple activated Michael acceptors, 1,3-dicarbonyls and ammonium acetate. Th
Publikováno v:
Current bioactive compounds
Tuberculosis (TB) remains one of the most deadly infectious diseases in the world, killing about 2 million people per year, and mostly affecting the worlds poorest population. The length of current regimens for treatment of TB is long (6-9 months) wi
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2007, pp.1323-1325. ⟨10.1055/s-2007-973906⟩
SYNLETT, 2007, pp.1323-1325. ⟨10.1055/s-2007-973906⟩
SYNLETT, Georg Thieme Verlag, 2007, pp.1323-1325. ⟨10.1055/s-2007-973906⟩
SYNLETT, 2007, pp.1323-1325. ⟨10.1055/s-2007-973906⟩
International audience; Molecular sieves have been found to promote a new fast, environmentally friendly and experimentally simple mul- ticomponent domino reaction from 1,3-dicarbonyls for the synthe- sis of pyrrolopiperazine and azasteroid-like scaf
Publikováno v:
ChemInform. 44
A metal-free and completely regioselective three-component synthesis of highly functionalized pyridines from 1,3-dicarbonyl derivatives and Michael acceptors has been achieved. Activated Michael acceptors, that is, β,γ-unsaturated α-oxo carbonyl d
Publikováno v:
ChemInform. 44
The reaction of activated Michael acceptors, 1,3-dicarbonyl derivatives and ammonium acetate allows for the preparation of a library of highly substituted bi- and tri(hetero)aryl pyridines.
Publikováno v:
ChemInform. 40
A simple metal-free, step-economic and selective access to pyridines from readily available substrates is reported, involving a flexible 4 A molecular sieves promoted Michael addition initiated domino three-component reaction between a 1,3-dicarbonyl
Publikováno v:
Chemical Communications
Chemical Communications, 2008, pp.4207-4209. ⟨10.1039/b805680c⟩
Chemical Communications, Royal Society of Chemistry, 2008, pp.4207-4209. ⟨10.1039/b805680c⟩
Chemical Communications, 2008, pp.4207-4209. ⟨10.1039/b805680c⟩
Chemical Communications, Royal Society of Chemistry, 2008, pp.4207-4209. ⟨10.1039/b805680c⟩
International audience; A simple metal-free, step-economic and selective access to pyr- idines from readily available substrates is reported, involving a flexible4A ̊ molecularsievespromotedMichaeladditioninitiated domino three-component reaction be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c417ae8b95b49b8e57db443889fd3e8
https://hal.science/hal-00677037/document
https://hal.science/hal-00677037/document
Publikováno v:
ChemInform. 37
A facile one-pot synthesis of functionalized pyrido[1,2-a]benzimidazoles is described via a molecular-sieves-promoted three-component domino reaction and in situ aerobic oxidation sequence from 1,3-dicarbonyls, aromatic o-diamines and unsaturated ald
Publikováno v:
ChemInform. 37
The aim of this mini-review is to present an overview of the high synthetic potential of Multicomponent Reactions (MCRs) involving the specific reactivity of easily accessible 1,3-dicarbonyl derivatives. The present contribution only focuses on seque