Synthesis of stemofurans C, L and T using organomanganese arene chemistry; Revised structure for stemofuran L
| Autor: | Dasan M. Thamattoor, Cassidy M. Madison, Christopher Y. Kim, William H. Miles, Daniel J. Sweitzer, Shelby D. Valent |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
010405 organic chemistry
Stereochemistry Organic Chemistry Cationic polymerization chemistry.chemical_element Regioselectivity Manganese 010402 general chemistry Cleavage (embryo) 01 natural sciences Biochemistry 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound chemistry Nucleophile Materials Chemistry Moiety Physical and Theoretical Chemistry Benzofuran Stemofuran L |
| Zdroj: | Journal of Organometallic Chemistry. 851:218-224 |
| ISSN: | 0022-328X |
| DOI: | 10.1016/j.jorganchem.2017.09.034 |
| Popis: | The synthesis of stemofurans C, L and T was achieved using organomanganese arene complexes. The critical carbon-carbon bond between the C-2 position of benzofuran and the arene was established in a regioselective manner directed by the cationic manganese tricarbonyl moiety. Oxidation of the resulting dienyl complexes and cleavage of the methyl ethers gave the desired stemofuran products. The spectroscopic data for the originally proposed structure for stemofuran L did not match the synthesized material, which prompted the synthesis of an isomer that did match the spectroscopic data. This revised structure has been proposed as the correct structure for stemofuran L. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect