Various synthetic schemes were used to prepare a number of new amino-thio- and sulfonyladamantane compounds. By a nucleophilic substitution on 1-bromoadamantane, 1-(p-nitrophenylthio)adamantane was prepared from p-nitrothiophenol; the amino- and sulfonyl- derivatives of this compound were also prepared. Silver tosylate was used to generate the 1-adamantyl carbonium ion from 1-bromoadamantane in a synthetically useful procedure for preparing 1-adamantylamides from nitriles. Three 1-(1-adamantylcarbinyl)-2,5-dialkylpyrroles were prepared by Knorr-Paal reactions and reduced to the corresponding pyrrolidines. Thio- and aminomethyl 1-adamantyl ketones were prepared from methyl and bromomethyl 1-adamantyl ketones, respectively. Aliphatic and aromatic oxiranes were reacted with 1-aminoadamantane in a bomb at elevated temperatures to give several new 2-(1-adamantylamino)ethanol derivatives.
| Identifer | oai:union.ndltd.org:BGMYU2/oai:scholarsarchive.byu.edu:etd-9156 |
| Date | 01 June 1970 |
| Creators | Argyle, Joseph Craig |
| Publisher | BYU ScholarsArchive |
| Source Sets | Brigham Young University |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | Theses and Dissertations |
| Rights | http://lib.byu.edu/about/copyright/ |
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