Enantioselective construction of ortho-sulfur- or nitrogen-substituted axially chiral biaryls and asymmetric synthesis of isoplagiochin D
Ortho-heteroatom-substituted axially chiral biaryls are valuable structures in synthetic and medicinal chemistry. Here, the authors established an efficient synthesis of these chiral structures via asymmetric cross-coupling.
| Główni autorzy: | , |
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| Format: | Artykuł |
| Język: | English |
| Wydane: |
Nature Portfolio
2022-08-01
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| Seria: | Nature Communications |
| Dostęp online: | https://doi.org/10.1038/s41467-022-32360-7 |