Abstract
Inspired by the high affinity of copper with DNA and RNA, a uracil-copper catalytic system was developed to promote ring-opening allylation of cyclopropanols with allylic alcohols under water-tolerant conditions. A new C-OH bond-breaking model can well resolve the trade-off between the need for acidic activators for C(allyl)-OH bond cleavage and the demand for strong basic conditions for generating homoenolates. Therefore, Morita-Baylis-Hillman alcohols, rather than their pre-activated versions, could be incorporated directly into dehydrative cross-coupling with cyclopropanols delivering water as the only by-product. A variety of functionalized δ,ϵ-unsaturated ketones were obtained in good-to-high yield with high E-selectivity.
Original language | English |
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Pages (from-to) | 1143-1149 |
Number of pages | 7 |
Journal | Chemical Science |
Volume | 15 |
Issue number | 3 |
DOIs | |
Publication status | Published - Dec 7 2023 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2024 The Royal Society of Chemistry.
ASJC Scopus Subject Areas
- General Chemistry