ISSN
Analysis
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Index « ISSN » - entrée « 0022-3263 »
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0022-2593 < 0022-3263 < 0022-3476  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 10.
Ident.Authors (with country if any)Title
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.
000C89 (2005) Stéphane Le Gac [France] ; Xianshun Zeng ; Olivia Reinaud ; Ivan JabinSynthesis and conformational study of the first triply bridged calix[6]azatubes.
000C92 (2005) Ulrich Darbost [France] ; Xianshun Zeng ; Michel Giorgi ; Ivan JabinOptically pure calix[6]tris-ammoniums: syntheses and host-guest properties toward neutral guests.
000D65 (2004) Xianshun Zeng [France] ; Nicolas Hucher ; Olivia Reinaud ; Ivan JabinA novel receptor based on a C3v-symmetrical PN3-calix[6]cryptand.
000D66 (2004) Ulrich Darbost [France] ; Michel Giorgi ; Olivia Reinaud ; Ivan JabinA novel C3v-symmetrical calix[6](aza)cryptand with a remarkably high and selective affinity for small ammoniums.
000E28 (2003) Ivan Jabin [France] ; Olivia ReinaudFirst C3v-symmetrical calix[6](aza)crown.
000F52 (2001) I. Jabin [France] ; G. Revial ; N. Monnier-Benoit ; P. NetchitaïloReaction of cyclohexanone benzylimines with ethylidenemalonate diesters. Diphenyl 2-ethylidenemalonate: a highly electrophilic synthetic equivalent of crotonic esters.
000F53 (2001) N. Hucher [France] ; Bernard Decroix [France] ; A. DaïchPi-aromatic and sulfur nucleophilic partners in cationic pi-cyclizations: intramolecular amidoalkylation and thioamidoalkylation cyclization via omega-carbinol lactams(1, 2).

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