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An Enantioselective Cross Dehydrogenative Coupling Catalysis Approach to Substituted Tetrahydropyrans
An enantioselective cross-dehydrogenative coupling (CDC) reaction to access tetrahydropyrans has been developed. This process combines in situ Lewis acid activation of a nucleophile in concert with the oxidative formation of a transient oxocarbenium electrophile, leading to a productive and highly e...
Gorde:
| Argitaratua izan da: | J Am Chem Soc |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6052785/ https://ncbi.nlm.nih.gov/pubmed/29714480 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jacs.8b03063 |
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