1,3-diphenylpropan-1,3-diamines .9. Reaction of alpha-chlorooxime ethers with alpha-lithiobenzylamines

Kaiser, A. and Wiegrebe, Wolfgang (1996) 1,3-diphenylpropan-1,3-diamines .9. Reaction of alpha-chlorooxime ethers with alpha-lithiobenzylamines. MONATSHEFTE FUR CHEMIE, 127 (6-7). pp. 763-774. ISSN 0026-9247, 1434-4475

Full text not available from this repository.

Abstract

The carbanions of the benzylamine derivatives 1-4 have been reacted with alpha-chlorooxime ether 5 in order to gel precursors of 1,3-diphenylpropane-1,3-diamines. Isonitrile 1 afforded the expected result, whereas lithiated benzamide 2 underwent oxidative dimerization and transmetallated chlorooxime derivative 5. Isoxazolidine 3 gave the condensation product 21 as a mixture of diastereomers; treatment of imine 4 led to the desired amine-oxime 15 in low yield.

Item Type: Article
Uncontrolled Keywords: 1,3-diphenylpropane-1,3-diamines; benzylamine carbanions; alpha-chloroacetophenoneoxime O-methyl ether
Subjects: 600 Technology > 615 Pharmacy
Divisions: Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Depositing User: Dr. Gernot Deinzer
Date Deposited: 06 Jul 2023 05:26
Last Modified: 06 Jul 2023 05:26
URI: https://pred.uni-regensburg.de/id/eprint/51685

Actions (login required)

View Item View Item