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The aminoindanol core as a key scaffold in bifunctional organocatalysts
The 1,2-aminoindanol scaffold has been found to be very efficient, enhancing the enantioselectivity when present in organocatalysts. This may be explained by its ability to induce a bifunctional activation of the substrates involved in the reaction. Thus, it is easy to find hydrogen-bonding organoca...
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| Vydáno v: | Beilstein J Org Chem |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Beilstein-Institut
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4901898/ https://ncbi.nlm.nih.gov/pubmed/27340443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.12.50 |
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