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Stereoselective synthesis of novel 2′-(S)-CCG-IV analogues as potent NMDA receptor agonists
We developed a versatile stereoselective route for the synthesis of new 2′-(S)-CCG-IV analogues. The route allows for late stage diversification and thereby provides access to a great variety of conformationally restricted cyclopropyl glutamate analogues. A selection of the 2′-(S)-CCG-IV analogues w...
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| Publicado no: | Eur J Med Chem |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8325387/ https://ncbi.nlm.nih.gov/pubmed/33383257 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejmech.2020.113099 |
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