I. The mechanism of aminations of halobenzenes. II. Quantum mechanical calculations of electrical effects of substituents in para-substituted anilines

I. The mechanism of aminations of halobenzenes. II. Quantum mechanical calculations of electrical effects of substituents in para-substituted anilines

PART I. The Mechanism of Aminations of Halobenzenes. An elimination-addition mechanism, probably involving a "benzyne" intermediate, was established for the rearrangements which often occur in the conversion of non-activated aryl halides to arylamines with metallic amides. The evidence fo...

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Bibliographic Details
Main Author: Semenow, Dorothy Ann
Format: Others
Published: 1955
Online Access:https://thesis.library.caltech.edu/260/1/Semenow_da_1955.pdf
Semenow, Dorothy Ann (1955) I. The mechanism of aminations of halobenzenes. II. Quantum mechanical calculations of electrical effects of substituents in para-substituted anilines. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/C8SK-WN09. https://resolver.caltech.edu/CaltechETD:etd-01212004-110215 <https://resolver.caltech.edu/CaltechETD:etd-01212004-110215>

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https://thesis.library.caltech.edu/260/1/Semenow_da_1955.pdf
Semenow, Dorothy Ann (1955) I. The mechanism of aminations of halobenzenes. II. Quantum mechanical calculations of electrical effects of substituents in para-substituted anilines. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/C8SK-WN09. https://resolver.caltech.edu/CaltechETD:etd-01212004-110215 <https://resolver.caltech.edu/CaltechETD:etd-01212004-110215>

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