Autor: |
Thomas R. Verhoeven, Anthony O. King, Paul J. Reider, Paul Davis, Edward G. Corley, James D. Carroll, Xiang Yi Bin, Marc Labelle, Robert Zamboni, Jacques Yves Gauthier, Robert D. Larsen |
Rok vydání: |
2010 |
Předmět: |
|
Zdroj: |
ChemInform. 27 |
ISSN: |
0931-7597 |
DOI: |
10.1002/chin.199637198 |
Popis: |
A general approach to the synthesis of a new class of LTD4 antagonists is presented. The key diarylpropane framework was prepared by Claisen−Schmidt condensation and selective reduction of the enone. Depending on the bridge to the 7-chloroquinaldine moiety, alkylation or Heck coupling methodology was developed. The chiral sulfides were introduced by asymmetric reduction of the diarylpropanone intermediates and subsequent inversion of the chiral center. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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