User:Etienne Robillard/Notebook/Fmoc protected phenoxyalkylamine synthesis

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The purpose of this page is to investigate the design and method of operation of novel psychotropic alkylamines and synthesis with Fmoc protected reagents, including primary and secondary amines as organocatalysts for development of synthetic pharmaceutical compounds with an aryl moeity, hence refered herein as N,N-substituted arylcyclohexylamines.

Microwave-activated peptide synthesis


N-Methyl-d-aspartate receptor; PCP binding site; MK-801; Tetrahydroisoquinolines, AHL,


  1. Rodríguez H, Suarez M, and Albericio F. A convenient microwave-enhanced solid-phase synthesis of short chain N-methyl-rich peptides. J Pept Sci. 2010 Mar;16(3):136-40. DOI:10.1002/psc.1209 | PubMed ID:20127857 | HubMed [Rodriguez-H-2012]
  2. Ludwig M, Hoesl CE, Höfner G, and Wanner KT. Affinity of 1-aryl-1,2,3,4-tetrahydroisoquinoline derivatives to the ion channel binding site of the NMDA receptor complex. Eur J Med Chem. 2006 Aug;41(8):1003-10. DOI:10.1016/j.ejmech.2006.03.005 | PubMed ID:16675066 | HubMed [Ludwig-M-Cornelia-E-CE-Hoesl-Klaus-T-KT-Wanner]
All Medline abstracts: PubMed | HubMed

See also

  • Lewis Acid Catalysed Pictet Spengler Formation of Substituted 1,2,3,4-Tetrahydroisoquinolines.