Publikation: Mode of alkylation of alcohols with O-cyclopropylmethyl trichloroacetimidate and O-cyclobutyl trichloroacetimidate
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2012
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Arkivoc. 2012(6), pp. 35-44. ISSN 1551-7004. eISSN 1551-7012
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Acid promoted alkylation of hydroxy group containing acceptors 3-14 with O-cyclopropylmethyl and O-cyclobutyl trichloroacetimidates 1 and 2, respectively, afforded ethers with cyclopropylmethyl, cyclobutyl, and homoallyl residues as a result of the rearrangement of the cation intermediates. The dependence of product formation on acceptor structure is discussed.
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ALI, Ibrahim A. I., Xiangming ZHU, El Sayed H. el ASHRY, Richard R. SCHMIDT, 2012. Mode of alkylation of alcohols with O-cyclopropylmethyl trichloroacetimidate and O-cyclobutyl trichloroacetimidate. In: Arkivoc. 2012(6), pp. 35-44. ISSN 1551-7004. eISSN 1551-7012BibTex
@article{Ali2012alkyl-21630,
year={2012},
title={Mode of alkylation of alcohols with O-cyclopropylmethyl trichloroacetimidate and O-cyclobutyl trichloroacetimidate},
number={6},
issn={1551-7004},
journal={Arkivoc},
pages={35--44},
author={Ali, Ibrahim A. I. and Zhu, Xiangming and Ashry, El Sayed H. el and Schmidt, Richard R.}
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