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Nucleophilic aliphatic substitution cyclic ether reactions

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]


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Aliphatic ethers

Cyclic ethers, reactions

Cyclic reactions

Ethere cyclic

Ethers cyclic

Ethers nucleophilicity

Ethers substitution reaction

Ethers, substituted

Nucleophiles substitution reactions

Nucleophilic aliphatic

Nucleophilic aliphatic cyclic ethers

Nucleophilic substitution reactions nucleophiles

Nucleophilic substitutions ethers

Substitution nucleophilic aliphatic

Substitution reactions nucleophile

Substitution reactions nucleophilic

Substitution reactions nucleophilic aliphatic

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