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.
Proceedings of the Iowa Academy of Science
©1934 Iowa Academy of Science, Inc.
Kirkpatrick, Willard H. and Gilman, Henry
"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