Direct conversion of alkenes into methyl-substituted cyclopropanes using an organoiron ethylidene transfer reagent
-
Add time:07/14/2019 Source:sciencedirect.com
(η5-C5H5)(CO)2FeCH(CH3)SPh (8) serves as a quite useful reagent for the transfer of ethylidene groups to alkenes to give methyl-substituted cyclopropanes in good yields. The reaction is accomplished by allowing 8 to react with an alkylating agent such as trimethyloxonium tetrafluoroborate or methyl fluorosulfonate in the presence of the alkene substrate. The active ethylidene transfer reagent is apparently a sulfonium salt which is too reactive to be isolated under normal conditions. In all cases, cyclopropanes are obtained stereospecifically with respect to the configuration of the starting alkenes, and with certain classes of substrates such as cis-disubstituted alkenes, the reaction also occurs with very high syn-stereoselectivity.
We also recommend Trading Suppliers and Manufacturers of 1-Chloro-2-(1-propenyl)cyclopropane (cas 74752-94-6). Pls Click Website Link as below: cas 74752-94-6 suppliers
Prev:Stereoselective Reduction of Cyclopropylalkaones Possessing a Difluoromethylenephosphonate Group at the Ring: Application to Stereoselective Synthesis of Novel Cyclopropane Nucleotide Analogues
Next:4-(Furan-2-yl)phenyl-containing polydithienylpyrroles as promising electrodes for high contrast and coloration efficiency electrochromic devices) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Stereoselective Reduction of Cyclopropylalkaones Possessing a Difluoromethylenephosphonate Group at the Ring: Application to Stereoselective Synthesis of Novel Cyclopropane Nucleotide Analogues07/13/2019
- A method for the synthesis of cyclopropanes by regiospecific and regioselective magnesium carbenoid 1,3-CH insertion as the key reactions07/12/2019


