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3,4-DIHYDRO--CARBOLINES: I. THE ALKYLATION OF...
Journal article

3,4-DIHYDRO--CARBOLINES: I. THE ALKYLATION OF 1-SUBSTITUTED N-ALKYL-3,4-DIHYDRO--CARBOLINE ANHYDRO BASES

Abstract

Methylation of the anhydro base derived from 1-methyl-3,4-dihydro-β-carboline methiodide is accompanied by ring opening and yields 3-[2-acetylindolyl]-β-ethyltrimethylammonium iodide, and not a 2,2-dialkyl-1-methylene-1,2,3,4-tetrahydro-β-carbolinium salt, as reported.

Authors

Gupta RN; Spenser ID

Journal

Canadian Journal of Chemistry, Vol. 40, No. 11, pp. 2041–2048

Publisher

Canadian Science Publishing

Publication Date

November 1, 1962

DOI

10.1139/v62-314

ISSN

0008-4042