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Stereoselective Synthesis of Cyclic Guanidines by Directed Diamination of Unactivated Alkenes
A method for a directed stereoselective guanidinylation of alkenes is described. The guanidine unit can be delivered as an intact fragment by a hydroxy or carboxy group, usually with a high level of stereocontrol. After the guanidine delivery, the directing group can be cleaved under exceptionally m...
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| Publicat a: | Org Lett |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5598158/ https://ncbi.nlm.nih.gov/pubmed/27778502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.6b02778 |
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