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Adam Daïcb < Adam Daïch < Adam Jakubowski  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 27.
[0-20] [0 - 20][0 - 27][20-26][20-40]
Ident.Authors (with country if any)Title
000045 (2016) Thomas Lepitre [France] ; Clement Denhez [France] ; Morgane Sanselme [France] ; Mohamed Othman [France] ; Ata Martin Lawson [France] ; Adam Daïch [France]Original Mitsunobu-Triggered Sequence Involved in a One-Pot Domino Process toward Tetracyclic Systems Bearing a Bis-N,O-acetal Junction.
000077 (2016) Dušan Berkeš [Slovaquie] ; Adam Daïch [France] ; Cécile Santos [France] ; Stéphanie Ballereau [France] ; Yves Génisson [France]Chemistry and Biology of HPAs: A Family of Ceramide Trafficking Inhibitors.
000081 (2016) Andrej Uriš ; Adam Daïch [France] ; Cécile Santos ; Laurence Fleury [France] ; Frédéric Ausseil [France] ; Frédéric Rodriguez ; Stéphanie Ballereau ; Yves Génisson [France] ; Dušan Berkeš [Slovaquie]Asymmetric Synthesis and Binding Study of New Long-Chain HPA-12 Analogues as Potent Ligands of the Ceramide Transfer Protein CERT.
000150 (2015) Cécile Santos [France] ; Laurence Fleury [France] ; Frédéric Rodriguez [France] ; Jozef Markus [Slovaquie] ; Dušan Berkeš [Slovaquie] ; Adam Daïch [France] ; Frédéric Ausseil [France] ; Cécile Baudoin-Dehoux [France] ; Stéphanie Ballereau [France] ; Yves Génisson [France]The CERT antagonist HPA-12: first practical synthesis and individual binding evaluation of the four stereoisomers.
000153 (2015) Ronan Le Goff [France] ; Arnaud Martel ; Morgane Sanselme ; Ata Martin Lawson ; Adam Daïch ; Sébastien ComesseSimple access to highly functional bicyclic γ- and δ-lactams: origins of chirality transfer to contiguous tertiary/quaternary stereocenters assessed by DFT.
000163 (2015) Aymen Ben Nejma [Tunisie] ; Asma Nguir [Tunisie] ; Hichem Ben Jannet [Tunisie] ; M'Hamed Ali Hamza [Tunisie] ; Adam Daïch [France] ; Mohamed Othman [France] ; Ata Martin Lawson [France]New septanoside and 20-hydroxyecdysone septanoside derivative from Atriplex portulacoides roots with preliminary biological activities.
000428 (2013) Ronan Le Goff [France] ; Ata Martin Lawson ; Adam Daïch ; Sébastien ComesseSynthesis of highly functionalized pyrrolidines as tunable templates for the direct access to (±)-coerulescine and the tricyclic core of martinellines.
000591 (2012) Peter Šafá ; Jozefína Žúžiová ; Štefan Marchalín [Slovaquie] ; Nadežda Pr Nayová [Slovaquie] ; Ubomír Švorc [Slovaquie] ; Viktor Vrábel [Slovaquie] ; Sergej Šesták [Slovaquie] ; Dubravko Rendi [Autriche] ; Vincent Tognetti [France] ; Laurent Joubert ; Adam Daïch [France]Combined Chemical, Biological and Theoretical DFT‐QTAIM Study of Potent Glycosidase Inhibitors Based on Quaternary Indolizinium Salts
000684 (2011) Sébastien Comesse [France] ; Arnaud Martel ; Adam DaïchDomino process optimized via ab initio study for an alternative access to bicyclic lactams.
000710 (2011) Iyad Allous [Syrie] ; Sébastien Comesse [France] ; Morgane Sanselme [France] ; Adam DaïchDiastereoselective Access to Tri‐ and Pentacyclic Spiro‐γ‐lactam‐oxindole Cores through a Tandem Aza‐Michael Initiated Ring Closure Sequence
000A24 (2008) Sébastien Comesse [France] ; Morgane Sanselme ; Adam DaïchNew and expeditious tandem sequence aza-Michael/intramolecular nucleophilic substitution route to substituted gamma-lactams: synthesis of the tricyclic core of (+/-)-martinellines.
000A33 (2008) Frédéric Pin [France] ; Sébastien Comesse ; Morgane Sanselme ; Adam DaïchA domino N-amidoacylation/aldol-type condensation approach to the synthesis of the topo-I inhibitor Rosettacin and derivatives.
000B18 (2007) Frédéric Pin [France] ; Sébastien Comesse ; Bernard Garrigues ; Stefan Marchalín ; Adam DaïchIntermolecular and intramolecular alpha-amidoalkylation reactions using bismuth triflate as the catalyst.
000C12 (2006) Anthony Pesquet [France] ; Adam Daïch ; Luc Van HijfteGeneral and versatile entry to 4,5-fused polycyclic imidazolones systems. Use of the tandem transposition/pi-cyclization of N-acyliminium species.
000D00 (2005) Anthony Pesquet [France] ; Adam Daïch [France] ; Bernard Decroix [France] ; Luc Van Hijfte [France]Acid-catalysed formation of tricyclic N,S-acetals in imidazolinone series based on the use of the unprecedented N-acyliminium ion cascade reaction involving transposition, heterocyclisation and π-cyclisation
000D09 (2005) Nicolas Hucher ; Anthony Pesquet ; Pierre Netchitaïlo ; Adam Daïch [France]Exocyclic–Endocyclic N‐Acyliminium Ion Equilibration via an Intramolecular α‐Thioamidoalkylation in the Synthesis of Fused N,S‐Heterocyclic Systems: Some New Parameters
000E44 (2003) Alain Fogain-Ninkam ; Adam Daïch ; Bernard Decroix [France] ; Pierre Netchitaïlo [France]Regioselective Reduction of 2‐(Arylideneamino)isoindole‐1,3‐diones − Synthesis of Alkaloid Analogues by N‐Acylhydrazonium Ion Aromatic π‐Cyclization
000E51 (2003) Armelle Cul [France] ; Anthony Pesquet [France] ; Adam Daïch [France] ; Abderrahim Chihab-Eddine [Maroc] ; Štefan Marchalín [Slovaquie]Evaluation of N‐hydroxymethylphthalimide in alkaline medium: Novel entry to the tricyclic [1,3]oxazepine core via an intramolecular π and O‐cationic cyclization
000F10 (2002) Jana Sikoraiová [Slovaquie] ; Štefan Marchalín [Slovaquie] ; Abderrahim Chihab-Eddine [Maroc] ; Adam Daïch [France]Diastereoselective access to chiral non‐racemic [1,3]oxazolo‐[2,3‐a]isoindol‐5‐one ring systems viaO‐cationic cyclization
001094 (2000) Abderrahim Chihab-Eddine [Maroc] ; Abderrahim Jilale [Maroc] ; Adam Daïch [France] ; Bernard Decroix [France]Reactivity of N‐benzyl‐3‐nitrophthalimide: A facile access to isoindolo[1,2‐d][3,5]benzothiazocine derivatives
001134 (1999) Alexander Bartovic [Slovaquie] ; Pierre Netchitaïlo [France] ; Adam Daïch [France] ; Bernard Decroix [France]A facile fused-dioxaza-ring synthesis from N -hydroxyphthalimide

List of associated KwdEn.i

Nombre de
documents
Descripteur
6Stereoisomerism
4Cyclization
3Models, Molecular
3Molecular Conformation
3Molecular Structure
3Nitrogen heterocycles
2Amides (chemistry)
2Lactams (chemistry)
2Protein Binding
2Protein-Serine-Threonine Kinases (antagonists & inhibitors)
2Pyrroles (chemical synthesis)
2Pyrroles (chemistry)
2Quinolines (chemical synthesis)
2Quinolines (chemistry)
2Structure-Activity Relationship
1Acetals (chemical synthesis)
1Acylation
1Acyliminium ion
1Alkaloids
1Amides
1Amides (chemical synthesis)
1Amides (metabolism)
1Amides (pharmacology)
1Aniline Compounds (chemical synthesis)
1Aniline Compounds (chemistry)
1Antioxidants (chemistry)
1Atriplex (chemistry)
1Atriplex (metabolism)
1Aza Compounds (chemistry)
1Bicyclo Compounds, Heterocyclic (chemical synthesis)
1Bicyclo Compounds, Heterocyclic (chemistry)
1Binding Sites (drug effects)
1Biological Transport
1Biological activity
1Catalysis
1Ceramides (chemistry)
1Ceramides (metabolism)
1Cholinesterases (chemistry)
1Cholinesterases (metabolism)
1Conformation analysis
1Density functional calculations
1Diastereoselectivity
1Dose-Response Relationship, Drug
1Ecdysterone (analogs & derivatives)
1Ecdysterone (chemistry)
1Ecdysterone (metabolism)
1Ecdysterone (pharmacology)
1Enzyme Inhibitors (chemical synthesis)
1Enzyme Inhibitors (chemistry)
1Enzyme Inhibitors (pharmacology)
1Enzyme inhibitors
1Gram-Negative Bacteria (drug effects)
1Gram-Positive Bacteria (drug effects)
1Heterocyclic Compounds with 4 or More Rings (chemical synthesis)
1Heterocyclic Compounds with 4 or More Rings (chemistry)
1Heterocyclic Compounds with 4 or More Rings (pharmacology)
1Heterocyclic Compounds, 3-Ring (chemical synthesis)
1Humans
1Hydrogen Bonding
1Imidazoles (chemical synthesis)
1Imidazoles (chemistry)
1Imidazolines (chemical synthesis)
1Isomerization
1Ketones (chemistry)
1Lactams (chemical synthesis)
1Ligands
1Magnetic Resonance Spectroscopy
1Michael addition
1Natural products
1Oxazoles (chemical synthesis)
1Oxazoles (chemistry)
1Piperidines (chemical synthesis)
1Piperidines (chemistry)
1Plant Extracts (chemistry)
1Plant Roots (chemistry)
1Plant Roots (metabolism)
1Polycyclic Hydrocarbons, Aromatic (chemical synthesis)
1Polycyclic Hydrocarbons, Aromatic (chemistry)
1Protein-Serine-Threonine Kinases (chemistry)
1Protein-Serine-Threonine Kinases (metabolism)
1Pyrrolidines (chemical synthesis)
1Pyrrolidines (chemistry)
1Pyrrolidinones (chemical synthesis)
1Pyrrolidinones (chemistry)
1Reduction
1Spiro compounds
1Sulfur heterocycles
1Thiophenes (chemistry)
1Topoisomerase I Inhibitors

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