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Nucleophilic aliphatic cyclic ethers

Silver(I) compounds are often used as promoters for substitution reactions of aliphatic halides with carbon nucleophiles. A cyclic (8-bromo ether 29 can be reacted with allyltrimethylsilane (30) imder the influence of AgBp4, yielding a mixture of ally-lated products 31 and 32 (Sch. 7) [15]. Product 31 is formed by direct substitution of the bromine atom in ether 29 by an allyl group and isomeric ether 32 arises from the carboxonium ion which is generated by debromination and subsequent [l,2]-hydrogen shift. A synthesis of optically active 4-allylazetidinone 33 (Ft = phthalimido) has also been achieved by employing the silver-promoted substitution reaction of 4-chloro-azetidinone 34 with allylsilane 30 [16]... [Pg.578]


See other pages where Nucleophilic aliphatic cyclic ethers is mentioned: [Pg.3]    [Pg.690]    [Pg.3]    [Pg.206]    [Pg.141]    [Pg.988]    [Pg.988]    [Pg.456]    [Pg.1577]    [Pg.80]    [Pg.329]    [Pg.271]    [Pg.251]    [Pg.988]    [Pg.22]   
See also in sourсe #XX -- [ Pg.43 , Pg.237 ]




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Aliphatic ethers

Ethere cyclic

Ethers cyclic

Ethers nucleophilicity

Nucleophilic aliphatic

Nucleophilic aliphatic substitution cyclic ether reactions

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