User:Etienne Robillard/Notebook/Fmoc protected phenoxyalkylamine synthesis

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(Microwave-activated peptide synthesis)
(Keywords)
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=== Keywords ===
=== Keywords ===
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N-Methyl-d-aspartate receptor; PCP binding site; MK-801; Tetrahydroisoquinolines, AHL,  
+
N-Methyl-d-aspartate receptor; PCP binding site; MK-801; Tetrahydroisoquinolines, AHL, NAND gate, Inverter
=== References ===
=== References ===

Revision as of 12:08, 29 January 2013

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.

Contents

Microwave-activated peptide synthesis

Keywords

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

References

  1. Rodríguez H, Suarez M, and Albericio F. . pmid:20127857. PubMed HubMed [Rodriguez-H-2012]
  2. Ludwig M, Hoesl CE, Höfner G, and Wanner KT. . pmid:16675066. PubMed 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.
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