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List of bibliographic references

Number of relevant bibliographic references: 17.
Ident.Authors (with country if any)Title
000033 (2013) Meral Goermen ; Ronan Le Goff ; Ata Martin Lawson ; Adam Daich ; Sebastien ComesseChemInform Abstract: Tandem Aza‐Michael/Spiro‐Ring Closure Sequence: Access to a Versatile Scaffold and Total Synthesis of (.+‐.)‐Coerulescine.
000034 (2013) Ronan Le Goff ; Ata Martin Lawson ; Adam Daich ; Sebastien ComesseChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.
000075 (2012) Iyad Allous ; Sebastien Comesse ; Morgane Sanselme ; Adam DaichChemInform Abstract: Diastereoselective Access to Tri‐ and Pentacyclic Spiro‐γ‐lactam‐oxindole Cores Through a Tandem Aza‐Michael Initiated Ring Closure Sequence.
000124 (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
000128 (2011) Moussa Saber ; Sebastien Comesse ; Vincent Dalla ; Adam Daich ; Morgane Sanselme ; Pierre NetchitailoChemInform Abstract: Formal [3 + 2]‐Cycloaddition‐Based Approach Using Ethoxymethylene Malonate Derivatives: Novel and Expedient Access to Functionalized N‐Acyliminium Precursors.
000313 (2009) Abderrahmane Hadou ; Abdulkareem Hamid ; Hilarion Mathouet ; Mohamed-Fadel Deida ; Adam DaichChemInform Abstract: An Easy Access to the Exocyclic Lactams Analogous of the Central Nervous System Active Tricyclic Nitroxapine, Mianserine and Chlothiapine Agents Using N‐Acyliminium Chemistry.
000580 (2005) Armelle Cul ; Adam Daich ; Bernard Decroix [France] ; Gerard Sanz ; Luc Van HijfteAccess to the New Isoindolo[1,3]benzothiazocinones via the Combination of N‐Acyliminium Chemistry and Friedel—Crafts Type π‐Cyclization.
000744 (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
000745 (2002) Jana Sikoraiova ; Abderrahim Chihab-Eddine ; Stefan Marchalin ; Adam DaichDiastereoselective Access to Chiral Non‐racemic [1,3]Oxazolo[2,3‐a]isoindol‐5‐one Ring Systems via O‐Cationic Cyclization.
000882 (2001) Abderrahim Chihab-Eddine ; Adam Daich ; Abderrahim Jilale ; Bernard Decroix [France]ChemInform Abstract: Reactivity of N‐Benzyl‐3‐nitrophthalimide: A Facile Access to Isoindolo[1,2‐d][3,5]benzothiazocine Derivatives.
000883 (2001) Milostav Chudik ; Stefan Marchalin ; Peter Knes ; Adam Daich ; Bernard Decroix [France]ChemInform Abstract: Facile Access to 6‐Substituted 1,4,5,7‐Tetrahydropyrrolo[3,4‐b]pyridines via Hantzsch Type Dimethyl 4‐Aryl‐2‐formyl‐6‐methyl‐1,4‐dihydropyridine‐3,5‐dicarboxylates.
000976 (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
000998 (2000) Milostav Chudík [Slovaquie] ; Štefan Marchalín [Slovaquie] ; Peter Knesl [Slovaquie] ; Adam Daich [France] ; Bernard Decroix [France]Facile access to 6‐substituted 1,4,5,7‐tetrahydropyrrolo[3,4‐b]‐pyridines via hantzsch type dimethyl 4‐aryl‐2‐formyl‐6‐methyl‐1,4‐dihydropyridine‐3,5‐dicarboxylates
000C29 (1998) P. Pigeon ; M. Othman ; P. Netchitailo ; Bernard Decroix [France]ChemInform Abstract: Selective Access to N‐Aryl or N‐Alkyl Derivatives of Isoindolo[2,1‐b][2,4]benzo(or thieno)diazepines.
000C30 (1998) A. Mamouni ; A. Daich ; Bernard Decroix [France]ChemInform Abstract: Palladium(II) Catalyzed Cyclization: A Facile Access to New Difunctionalized Thieno[3,2‐f]indolizine.
000D52 (1997) P. Pigeon ; Bernard Decroix [France]ChemInform Abstract: A New Access to Isoindolo(2,1‐b)(2,4)benzodiazepines Through an N‐ Acyliminium Ion‐Amide Cyclization.
001189 (1991) Bernard Decroix [France] ; J. MorelChemInform Abstract: Intramolecular Cyclizations: Access to 9‐Oxo‐4H,9H‐pyrrolo(1,2‐a) thieno(2,3‐d)pyridine and 4‐Oxo‐4H,9H‐pyrrolo(1,2‐a)thieno(3,2‐d) pyridine. Synthesis of Pyrrolo(1,2‐a)thieno(3,2‐e)(1,4)diazepine and Pyrrolo(1,2‐a)thieno(2,3‐e)(1,4)diazepine.

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