Abstract
We report a new iron-catalyzed I/Zn-exchange allowing to convert primary or tailored secondary alkyl iodides into the corresponding alkylzinc iodides. In the presence of a remote double bond at position 5, diastereoselective ring closures are observed. Quenching of these zinc reagents, after transmetalation to copper species (with CuCN center dot 2LiCl) or under Pd-catalysis, with typical electrophiles (allyl bromides, acid chlorides or aryl iodides) gave various polyfunctional products.
Item Type: | Journal article |
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Faculties: | Chemistry and Pharmacy > Department of Chemistry |
Subjects: | 500 Science > 540 Chemistry |
URN: | urn:nbn:de:bvb:19-epub-106946-4 |
ISSN: | 1615-4150 |
Language: | English |
Item ID: | 106946 |
Date Deposited: | 11. Sep 2023, 13:45 |
Last Modified: | 04. Oct 2023, 16:32 |
DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 491502892 |