Pyridine and Quinoline Derivates of Dibenzofuran, and Their Physiological Properties

Authors

Willard H. Kirkpatrick, Iowa State CollegeFollow
Henry Gilman, Iowa State CollegeFollow

Document Type

Research

Abstract

A study is in progress of the physiological properties, particularly the narcotic action, of amino and substituted aminodibenzofurans and their nuclear reduction products. The amino compounds in many cases are cyclicized to give pyridino-dibenzofurans. Simple illustrations of parent types are the quinolines derived by Shraup and other syntheses from the amino dibenzofurans and their reduction products. The nitrogen cycles have been extended to include bridging of rings which vary both in kind and position of substituents as well as in degree of nuclear reduction.

Publication Date

1934

Journal Title

Proceedings of the Iowa Academy of Science

Volume

41

Issue

1

First Page

172

Last Page

172

Copyright

©1934 Iowa Academy of Science, Inc.

Language

en

File Format

application/pdf

Recommended Citation

Kirkpatrick, Willard H. and Gilman, Henry (1934) "Pyridine and Quinoline Derivates of Dibenzofuran, and Their Physiological Properties," Proceedings of the Iowa Academy of Science, 41(1), 172-172.
Available at: https://scholarworks.uni.edu/pias/vol41/iss1/57