Naphthalenophane formaldehyde acetals as candidate structures for the generation of dynamic libraries via transacetalation processes
Authors:
- Albert RuggiARAlbert Ruggi
- Roberta CacciapagliaRCRoberta Cacciapaglia
- Stefano Di StefanoSSStefano Di Stefano
- Enrico BodoEnrico Bodo
- Franco UgozzoliFUFranco Ugozzoli
- 1 April 2013
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 69 (13) , 2767-2774
Abstract
No abstract availableKeywords
This publication has 65 references indexed in Scilit:
- Dynamic Combinatorial Chemistry Employing Boronic Acids/Boronate Esters Leads to Potent Oxygenase InhibitorsAngewandte Chemie International Edition, 2012
- Macrocyclic depolymerization of arylene-ethynylene copolymers: a dynamic combinatorial methodChemical Communications, 2012
- Ternary resin-bound dynamic combinatorial chemistryChemical Communications, 2011
- Dynamic combinatorial development of a neutral synthetic receptor that binds sulfate with nanomolar affinity in aqueous solutionChemical Communications, 2011
- Discovery of Linear Receptors for Multiple Dihydrogen Phosphate Ions Using Dynamic Combinatorial ChemistryJournal of the American Chemical Society, 2011
- Macrocycle or Cage? The Presence or Absence of Ca2+ Template Ions Controls the Equilibrium in an Oligoimine Dynamic Combinatorial LibraryEuropean Journal of Organic Chemistry, 2011
- A Bidentate Halogen‐Bonding Bromoimidazoliophane Receptor for Bromide Ion Recognition in Aqueous MediaAngewandte Chemie International Edition, 2011
- Reversible Thiazolidine Exchange: A New Reaction Suitable for Dynamic Combinatorial ChemistryOrganic Letters, 2009
- Scalable Total Synthesis and Biological Evaluation of Haouamine A and Its AtropisomerJournal of the American Chemical Society, 2009
- Ultrafast Photoinduced Electron Transfer within a Self-Assembled Donor−Acceptor SystemThe Journal of Physical Chemistry A, 2005