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Synthesis of Conformationally Locked Versions of Puromycin Analogues
[Image: see text] Conformationally locked North and South versions of puromycin analogues built on a bicyclo[3.1.0]hexane pseudosugar template were synthesized. The final assembly of the products was accomplished by the Staudinger-Vilarrasa coupling of the corresponding North (2 and 3) and South (6...
Gorde:
| Egile Nagusiak: | , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2008
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2765511/ https://ncbi.nlm.nih.gov/pubmed/18991379 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo8016132 |
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