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 Netchitailo | Regioselective 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 Decroix | ChemInform 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. Decroix | ChemInform 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. Decroix | ChemInform 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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