Highly efficient CC bond formation in the two-photon chemistry of 1,8-bis(substituted-methyl)naphthalenes by direct excitation of photoactive leaving groups
-
Add time:09/08/2019 Source:sciencedirect.com
High efficiency in the two-photon intramolecular CC bond formation to the two-photon product acenaphthene (4), obtained in a maximum yield of 72%, was achieved by direct activation of two separate leaving groups of 1,8-bis(phenoxymethyl)- (1a), 1,8-bis(phenylthiomethyl)- (1b), and 1,8-bis(phenylselenomethyl)-naphthalenes (1c) during KrF excimer laser (248 nm) and of 1,8-bis(4-benzoylphenoxymethyl)- (1d), 1,8-bis(3-benzoylphenoxymethyl)- (1e), and 1,8-bis(2-naphthoxymethyl)naphthalenes (1f) during XeF excimer laser (351 nm) photolyses.
We also recommend Trading Suppliers and Manufacturers of 1,8-Bis(phenylthio)-9,10-anthracenedione (cas 13676-91-0). Pls Click Website Link as below: cas 13676-91-0 suppliers
Prev:Research paperSynthesis, characterization, aggregation, fluorescence and antioxidant properties of bearing (4-(methylthio)phenylthio) tetra substituted phthalocyanines
Next:NoteShort syntheses of 8-substituted 8′-[1-(1′-phenylthio)ferrocenyl]-1,1′-binaphthyls from Suzuki coupling reactions. A strategy for generating new chiral ligands and charge-transfer complexes) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- NoteShort syntheses of 8-substituted 8′-[1-(1′-phenylthio)ferrocenyl]-1,1′-binaphthyls from Suzuki coupling reactions. A strategy for generating new chiral ligands and charge-transfer complexes09/09/2019
- Research paperSynthesis, characterization, aggregation, fluorescence and antioxidant properties of bearing (4-(methylthio)phenylthio) tetra substituted phthalocyanines09/07/2019
- Parallel and perpendicular stacking of ferrocene rings.: Syntheses, X-ray structures, and electrochemistry of 1,8-bis-[1-(1′-phenylthio)ferrocenyl]naphthalene and 8,8′-bis-[1-(1′-phenylthio)ferrocenyl]-1,1′-binaphthyl09/06/2019


