2023
DOI: 10.1016/j.tetlet.2022.154257
|View full text |Cite
|
Sign up to set email alerts
|

Ring opening of cyclopropyl ketones with 1,3-diketones for the synthesis of 1,6-diketone derivatives

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 59 publications
0
1
0
Order By: Relevance
“… 4 Recently, we developed scandium triflate catalyzed O-selective nucleophilic ring-opening of D–A cyclopropanes with 1,3-cyclodiones, 5 b where the ring-opening products 1,3-cyclodione enol ether derivatives were obtained in good to excellent yields ( Scheme 1a ). In continuation of our research interests in the reactions between 1,3-dicarbonyl compounds and D–A cyclopropanes, 5 herein, we disclose the asymmetric version of the ring opening reactions of D–A cyclopropanes with 1,3-cyclodiones ( Scheme 1b ).…”
mentioning
confidence: 96%
“… 4 Recently, we developed scandium triflate catalyzed O-selective nucleophilic ring-opening of D–A cyclopropanes with 1,3-cyclodiones, 5 b where the ring-opening products 1,3-cyclodione enol ether derivatives were obtained in good to excellent yields ( Scheme 1a ). In continuation of our research interests in the reactions between 1,3-dicarbonyl compounds and D–A cyclopropanes, 5 herein, we disclose the asymmetric version of the ring opening reactions of D–A cyclopropanes with 1,3-cyclodiones ( Scheme 1b ).…”
mentioning
confidence: 96%