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- W2022700153 abstract "A highly efficient synthesis based on inexpensive and readily available starting material towards the pharmacologically interesting class of substituted 2,3,4,7-tetrahydro-1H-azepines via a ring-closing metathesis (RCM) approach employing Grubbs catalysts 1 and 2 is described. The influence of the substituents R1 and R2 on the outcome of the RCM reaction is discussed. The seemingly first example of an RCM approach towards seven-membered azacycles bearing a substituent at the alkene moiety utilizing Grubbs catalyst 1 is presented." @default.
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- W2022700153 date "2006-02-01" @default.
- W2022700153 modified "2023-10-09" @default.
- W2022700153 title "Facile synthesis of substituted 2,3,4,7-tetrahydro-1H-azepines via ring-closing metathesis" @default.
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- W2022700153 doi "https://doi.org/10.1016/j.tet.2005.11.049" @default.
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