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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...

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Bibliographische Detailangaben
Hauptverfasser: Saneyoshi, Hisao, Michel, Benoît Y., Choi, Yongseok, Strazewski, Peter, Marquez, Victor E.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2008
Schlagworte:
Online Zugang: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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