| Autor: |
Sbi, Sanae, Mkpenie, Victor, Tanemura, Kiyoshi, Rohand, Taoufik |
| Předmět: |
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| Zdroj: |
Synlett; 2020, Vol. 31 Issue 9, p903-906, 4p |
| Abstrakt: |
A variety of 1,3-disubstituted naphthalenes have been prepared by palladium-catalyzed annulation of (o -ethynylphenyl)acetyl chloride with design of a new synthetic strategy by Stille coupling using functionalized organostannanes. The method affords excellent yields of the substituted naphthalenes and accommodates a wide variety of functional groups under mild conditions. Mechanistic studies show intramolecular cyclization as a major step following C–C bond coupling. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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