Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
American Chemical Society
2020-10-01
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| Series: | ACS Omega |
| Online Access: | https://doi.org/10.1021/acsomega.0c04181 |
| _version_ | 1818426546785878016 |
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| author | Adrien Dumas Jean-Baptiste Garsi Guillaume Poissonnet Stephen Hanessian |
| author_facet | Adrien Dumas Jean-Baptiste Garsi Guillaume Poissonnet Stephen Hanessian |
| author_sort | Adrien Dumas |
| collection | DOAJ |
| first_indexed | 2024-12-14T14:31:33Z |
| format | Article |
| id | doaj.art-2236469ca48441e6a2f6f5ef289bfa52 |
| institution | Directory Open Access Journal |
| issn | 2470-1343 |
| language | English |
| last_indexed | 2024-12-14T14:31:33Z |
| publishDate | 2020-10-01 |
| publisher | American Chemical Society |
| record_format | Article |
| series | ACS Omega |
| spelling | doaj.art-2236469ca48441e6a2f6f5ef289bfa522022-12-21T22:57:47ZengAmerican Chemical SocietyACS Omega2470-13432020-10-01542275912760610.1021/acsomega.0c04181Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive AnaloguesAdrien Dumas0Jean-Baptiste Garsi1Guillaume Poissonnet2Stephen Hanessian3Department of Chemistry, Université de Montréal, Montréal, QC, CanadaDepartment of Chemistry, Université de Montréal, Montréal, QC, CanadaCentEX Chemistry, Institut de Recherches Servier, Suresnes, FranceDepartment of Chemistry, Université de Montréal, Montréal, QC, Canadahttps://doi.org/10.1021/acsomega.0c04181 |
| spellingShingle | Adrien Dumas Jean-Baptiste Garsi Guillaume Poissonnet Stephen Hanessian Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues ACS Omega |
| title | Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues |
| title_full | Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues |
| title_fullStr | Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues |
| title_full_unstemmed | Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues |
| title_short | Ni-Catalyzed Reductive and Merged Photocatalytic Cross-Coupling Reactions toward sp3/sp2‑Functionalized Isoquinolones: Creating Diversity at C‑6 and C‑7 to Address Bioactive Analogues |
| title_sort | ni catalyzed reductive and merged photocatalytic cross coupling reactions toward sp3 sp2 functionalized isoquinolones creating diversity at c 6 and c 7 to address bioactive analogues |
| url | https://doi.org/10.1021/acsomega.0c04181 |
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