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Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction
Enantiomerically pure β-aminoalcohols, produced through an organocatalytic Mannich reaction, were subjected to an Ugi multicomponent reaction under classical or Lewis acid-promoted conditions with diastereoselectivities ranging from moderate to good. This approach represents a step-economical path t...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Beilstein J Org Chem |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Beilstein-Institut
2016
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4734417/ https://ncbi.nlm.nih.gov/pubmed/26877816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.12.15 |
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