Carbonium ion rearrangements in reactions of cyclopropylcarbinyl and cyclobutyl derivatives

Carbonium ion rearrangements in reactions of cyclopropylcarbinyl and cyclobutyl derivatives

1-Methylcyclopropylcarbinylamine and 1-methylcyclobutylamine on treatment with aqueous nitrous acid gave only 1-methylcyclobutanol, while [beta]-methylallylcarbinylamine gave predominantly [beta]-methylallylcarbinol and 1-methylcyclobutanol, with smaller amounts of of [alpha]-methyl-[beta]-methylall...

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Bibliographic Details
Main Author: Cox, Eugene Floyd
Format: Others
Published: 1955
Online Access:https://thesis.library.caltech.edu/4757/1/Cox_ef_1955.pdf
Cox, Eugene Floyd (1955) Carbonium ion rearrangements in reactions of cyclopropylcarbinyl and cyclobutyl derivatives. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/NS0V-W084. https://resolver.caltech.edu/CaltechETD:etd-12042003-093721 <https://resolver.caltech.edu/CaltechETD:etd-12042003-093721>

Internet

https://thesis.library.caltech.edu/4757/1/Cox_ef_1955.pdf
Cox, Eugene Floyd (1955) Carbonium ion rearrangements in reactions of cyclopropylcarbinyl and cyclobutyl derivatives. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/NS0V-W084. https://resolver.caltech.edu/CaltechETD:etd-12042003-093721 <https://resolver.caltech.edu/CaltechETD:etd-12042003-093721>

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