User:Etienne Robillard/Notebook/Fmoc protected phenoxyalkylamine synthesis

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as organocatalysts for development of synthetic pharmaceutical compounds with an aryl moeity, hence
as organocatalysts for development of synthetic pharmaceutical compounds with an aryl moeity, hence
refered herein as N,N-substituted arylcyclohexylamines.
refered herein as N,N-substituted arylcyclohexylamines.
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=== Microwave-activated peptide synthesis ===
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* NB: the electromagnetic radio-frequency range most typical wireless devices operates under the FCC standard for communication devices is 2.4 ghz.
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* http://www.pharmainfo.net/reviews/new-era-field-synthetic-chemistry-microwave-assisted-synthesis
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* http://www.dddmag.com/articles/2011/08/microwave-peptide-synthesis
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=== Keywords ===
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N-Methyl-d-aspartate receptor; PCP binding site; MK-801; Tetrahydroisoquinolines
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=== References ===
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<biblio>
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#Rodriguez-H-2012 pmid=20127857
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#Ludwig-M-Cornelia-E-CE-Hoesl-Klaus-T-KT-Wanner pmid=16675066
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</biblio>
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=== See also ===
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* Lewis Acid Catalysed Pictet Spengler Formation of Substituted 1,2,3,4-Tetrahydroisoquinolines.

Revision as of 19:49, 25 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

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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