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Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization
[Image: see text] Functionalized 4- and 6-azaindolines are accessible with high levels of enantioselectivity by the cation-directed cyclization of aminopyridine-derived imines via phase-transfer catalysis. The extension of this methodology to diastereoselective cyclizations is also described.
Na minha lista:
| Foilsithe in: | Org Lett |
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| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
American Chemical Society
2016
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| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5086784/ https://ncbi.nlm.nih.gov/pubmed/27709963 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.6b02744 |
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