Universal Rink–isonitrile resin: application for the traceless synthesis of 3-acylamino imidazo[1,2-a]pyridines
- 18 March 2001
- journal article
- research article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 42 (12), 2269-2271
- https://doi.org/10.1016/s0040-4039(01)00159-9
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Multicomponent Reactions with IsocyanidesAngewandte Chemie-International Edition, 2000
- The reaction of cyclohexyl isocyanide and dimethyl acetylenedicarboxylate with aldehydes: a novel synthesis of 2-aminofuran derivativesChemical Communications, 2000
- A novel dealkylation affording 3-aminoimidazo[1,2-a]pyridines: access to new substitution patterns by solid-phase synthesisTetrahedron Letters, 2000
- Enhanced Diastereoselectivity in the Asymmetric Ugi Reaction Using a New “Convertible” IsonitrileThe Journal of Organic Chemistry, 1998
- Novel safety-catch linker and its application with a Ugi/De-BOC/Cyclization (UDC) strategy to access carboxylic acids, 1,4-benzodiazepines, diketopiperazines, ketopiperazines and dihydroquinoxalinonesTetrahedron Letters, 1998
- Mild N-dealkylation of tertiary, benzylic amines with acid chlorides: Application to solid-phase chemistryTetrahedron Letters, 1998
- Postcondensation Modifications of Ugi Four-Component Condensation Products: 1-Isocyanocyclohexene as a Convertible Isocyanide. Mechanism of Conversion, Synthesis of Diverse Structures, and Demonstration of Resin CaptureJournal of the American Chemical Society, 1996
- Color test for detection of free terminal amino groups in the solid-phase synthesis of peptidesAnalytical Biochemistry, 1970