Pd-catalyzed oxa-[4+n] dipolar cycloaddition using 1,4-O/C dipole synthons for the synthesis of O-heterocycles
- Authors
- Cho, Ho-Jun; Kim, Ju Hyun
- Issue Date
- Dec-2023
- Publisher
- Royal Society of Chemistry
- Citation
- Organic and Biomolecular Chemistry, v.21, no.48, pp 9507 - 9518
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Organic and Biomolecular Chemistry
- Volume
- 21
- Number
- 48
- Start Page
- 9507
- End Page
- 9518
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/69000
- DOI
- 10.1039/d3ob01619f
- ISSN
- 1477-0520
1477-0539
- Abstract
- Transition metal-catalyzed dipolar cycloaddition is one of the most efficient and powerful synthetic strategies to produce diverse heterocycles. In particular, for the construction of oxygen-containing heterocycles, which are valuable structural motifs found in pharmaceuticals and natural compounds, transition metal-catalyzed oxa-dipolar cycloaddition using an oxygen-containing dipole has emerged as a promising method. In recent years, the 1,4-O/C dipole synthons 2-alkylidenetrimethylene carbonate and 2-hydroxymethylallyl carbonate have been developed and successfully applied to palladium-catalyzed oxa-[4 + n] dipolar cycloadditions with diverse dipolarophiles. In this review, we summarize recent advances in palladium-catalyzed oxa-[4 + n] dipolar cycloadditions using 1,4-O/C dipoles including asymmetric catalysis and divergent catalysis toward five- to nine-membered O-heterocycles.
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