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Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer–Schuster Rearrangement, Anti-Michael Addition/C((sp(3)))–H Functionalization, and Azacyclization
[Image: see text] A one-pot, sequential Meyer–Schuster (MS) rearrangement of oxindole-derived propargyl alcohols to the corresponding α,β-unsaturated enones and their anti-Michael addition, followed by intramolecular azacyclization is described in a highly regioselective manner using Ca(OTf)(2) as t...
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| Pubblicato in: | ACS Omega |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Chemical Society
2018
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6044873/ https://ncbi.nlm.nih.gov/pubmed/30023853 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsomega.8b00147 |
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