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Highly Torquoselective Electrocyclizations and Competing 1,7-Hydrogen Shifts of 1-Azatrienes with Silyl-Substitution at the Allylic Carbon
[Image: see text] Highly torquoselective electrocyclizations of chiral 1-azatrienes are described. These 1-azatrienes contain an allylic stereocenter that is substituted with a silyl group and are derived in situ from condensation of γ-silyl-substituted enals with vinylogous amides. The ensuing ster...
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| Vydáno v: | Org Lett |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4547485/ https://ncbi.nlm.nih.gov/pubmed/25859907 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.5b00727 |
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