Abstract
A regioselective protocol for the synthesis of cyclopropyl derivatives that relies on Brookhart acid-catalyzed dehydrative coupling over substituted cyclopropylcarbinols without rearrangement is reported herein. The reactions proceed promptly at 25 °C with only 2.0 mol % catalyst loading and produce the cyclopropyl derivatives in excellent yields. This method is well tolerated with a vast range of cyclopropylcarbinols including aliphatic cyclopropylcarbinols, where no elimination product was obtained, demonstrating the protocol’s utility. Further, the Hammett correlation suggested the formation of a cyclopropylcarbinyl cation followed by a coupling reaction. An extremely effective gram-scale reaction has also been demonstrated with a high turnover number.
| Original language | English |
|---|---|
| Pages (from-to) | 6886-6901 |
| Number of pages | 16 |
| Journal | Journal of Organic Chemistry |
| Volume | 87 |
| Issue number | 10 |
| DOIs | |
| State | Published - 20 May 2022 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 American Chemical Society.
ASJC Scopus subject areas
- Organic Chemistry
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