Cristau, PierreVors, Jean-PierreZhu, Jieping2010-11-252010-11-252010-11-25200610.1002/qsar.200540214https://infoscience.epfl.ch/handle/20.500.14299/58450The title cyclophanes, such as I, were prepd. via a Ugi-4CR four component reaction and subsequent macrocyclization of the resulting amides using intramol. SNAr reactions. [on SciFinder (R)]Addition reaction (Ugi; synthesis of cyclopeptide alkaloid-like para-cyclophanes by combined use of Ugi-4CR and intramol. SNAr reaction); Substitution reaction (arom.; synthesis of cyclopeptide alkaloid-like para-cyclophanes by combined use of Ugi-4CR and intramol. SNAr reaction); Peptides Role: PNU (Preparationunclassified)PREP (Preparation) (cyclicalkaloidal; synthesis of cyclopeptide alkaloid-like para-cyclophanes by combined use of Ugi-4CR and intramol. SNAr reaction); Alkaloids Role: PNU (Preparationunclassified)PREP (Preparation) (cyclopeptidyl; synthesis of cyclopeptide alkaloid-like para-cyclophanes by combined use of Ugi-4CR and intramol. SNAr reaction)cyclic peptide alkaloid paracyclophane synthesis Ugi reaction; intramol arom substitution cyclic peptide alkaloid paracyclophane synthesisRapid synthesis of cyclopeptide alkaloid-like para-cyclophanes by combined use of Ugi-4CR and intramolecular SNAr reactiontext::journal::journal article::research article