Divergent Reactions of α-Diazo 1,3-Dicarbonyl Compounds with Allylic Carbonates Involving Ketene versus Carbene Intermediates Enabled by Cooperative Rh(II)/Pd(0) Dual Catalysis
A cooperative Rh(II)/Pd(0) dual-catalysis strategy that enabled divergent reactions of α-diazo 1,3-dicarbonyl compounds with allylic carbonates involving ketene versus carbene intermediates is described. The efficient synthesis of α-quaternary allylated β-keto-esters was accomplished by the Rh(II)/Pd(0) dual-catalysis allylic alkylation of α-diazo 1,3-dicarbonyl compounds. Alternatively, an unprecedented (1+4) annulation of α-diazo 1,3-dicarbonyl compounds with 2-(hydroxymethyl)allyl carbonates via Rh(II)/Pd(0) dual catalysis was also successfully developed, affording a wide variety of α-quaternary tetrahydrofurans in good to high yields.
Authors
- Zi‐Sheng Chen (ORCID: https://orcid.org/0000-0001-8778-8889)
- Yuhua Song (ORCID: https://orcid.org/0000-0002-2583-850X)
- De-Xin Song
- Ke‐Gong Ji (ORCID: https://orcid.org/0000-0001-5707-894X)
- Fang Yang (ORCID: https://orcid.org/0000-0001-6338-8100)
- Xiaoyan Huang (ORCID: https://orcid.org/0000-0001-7322-2796)
- Heng-Hua Huang
Institutions
- Northwest A&F University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2024-09-09
- DOI
- https://doi.org/10.1021/acs.orglett.4c02947
- Citations
- 7
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 1.75
Funders
- National Natural Science Foundation of China
- Northwest A and F University