Serveur d'exploration sur la visibilité du Havre - Curation (Istex)

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List of bibliographic references

Number of relevant bibliographic references: 35.
[0-20] [0 - 20][0 - 35][20-34][20-40]
Ident.Authors (with country if any)Title
000020 (2004) Alain Fogain-Ninkam ; Adam Daich ; Bernard Decroix ; Pierre NetchitailoRegioselective Reduction of 2‐(Arylideneamino)isoindole‐1,3‐diones — Synthesis of Alkaloid Analogues by N‐Acylhydrazonium Ion Aromatic π‐Cyclization.
000043 (1999) Mohamed Othman ; Pascal Pigeon ; Bernard DecroixChemInform Abstract: Synthesis and Reduction of Thieno[2′,3′(3′,2′ or 3′,4′):5,6]azocino[2,1‐a]isoindole‐7,13‐diones.
000075 (1995) Dusan Berkes [France] ; Nathalie Bar [France] ; Bernard Decroix [France]Stereoselective reduction of new fused azoninones with a bridgehead nitrogen
000089 (1995) D. Berkes ; N. Bar ; B. DecroixChemInform Abstract: Stereoselective Reduction of New Fused Azoninones with a Bridgehead Nitrogen.
000099 (1998) Mohamed Othman [France] ; Pascal Pigeon [France] ; Bernard Decroix [France]Synthesis and reduction of thieno[2′,3′(3′,2′ or 3′,4′):5,6]‐azocino[2,1‐a]isoindole‐7, 13‐diones
000112 (1995) D. Berkes ; B. DecroixChemInform Abstract: Synthesis of Piperidinothienoazepinones, Methano‐thienoazecinone and Study of Their Stereoselective Reduction.
000137 (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
000138 (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
000298 (2007) Quentin Bénard [France] ; Magali Fois ; Michel Grisel [France] ; Céline Picard [France]On the Influence of Polymer Surface Layer Thickness on the Adhesion of Composite Assembly. Differences between Initial State and Thermal Ageing
000321 (1999) Nicolas Hucher [France] ; Adam Dai Ch [France] ; Pierre Netchitai Lo [France] ; Bernard Decroix [France]Newly intramolecular α-amidoalkylation cyclisation: Use of the N -acyliminium ion with a sulfur atom as a nucleophile
000327 (2001) Abderrahim Chihab-Eddine [Maroc] ; Adam Da Ch [France] ; Abderrahim Jilale [Maroc] ; Bernard Decroix [France]Synthesis and reactivity of (1 S )- N -(1-phenylethyl)maleimide towards nucleophiles: an application to preparation of chiral pyrroloisothiochroman and pyrrolobenzo[ d ]thiepine based on π-cationic cyclization
000398 (2001) Anita Guesdon [France] ; Alain Fogain-Ninkam [France] ; Bernard Decroix [France] ; Pierre Netchitaïlo [France]Synthesis of 1,3,4‐oxa(or thia)diazaheterocycles starting from 2‐(pyrrol‐1'‐y1)phthalimide
000697 (2003) Alain Fogain-Ninkam ; Adam Daïch ; Bernard Decroix ; Pierre Netchitaïlo [France]Regioselective Reduction of 2‐(Arylideneamino)isoindole‐1,3‐diones − Synthesis of Alkaloid Analogues by N‐Acylhydrazonium Ion Aromatic π‐Cyclization
000812 (2006) Turbulent drag reduction by surfactants
000831 (1984) A. Godet [France] ; G. Roussel [France] ; M. Thebault [France]Frictional behaviour of experimental synthetic and semi‐synthetic gear oils
000846 (1991) T. Jouenne [France] ; L. Bertin [France] ; G. Charriere [France] ; G. A. Junter [France]Electrochemical assessment of Escherichia coli survival in natural water
000918 (2000) A. Benamar [France]Dynamic pile response using two pile-driving techniques
000987 (1988) 12. What Transport Arrangements Should We Make
000B18 (1999) V. Dalla [France] ; J. P. Catteau [France] ; P. Pale [France]Mechanistic rationale for the NaBH4 reduction of α-keto esters
000B58 (1984) Guy-Alain Junter [France]Potentiometric detection and study of bacterial activity
000B66 (2001) Gilbert Revial [France] ; Ivan Jabin [France] ; Michaël Redolfi [France] ; Michel Pfau [France]Enantioselective imine Michael reaction for the preparation of the (8′ R ,8a′ S )-8,8a′-dimethyl-1′,3′,4′,7′,8′,8a′-hexahydrospiro[1,3-dioxolane-2,2′(6′ H )naphthalen]-6′-one building block. A formal synthesis of (+)-valencenol

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