Author:
Ferles Miloslav,Šilhánková Alexandra,Kafka Stanislav,Taufmann Petr,Motáček Tomáš
Abstract
Reduction of ethyl esters of ω-(1,2,3,4-tetrahydro-2-isoquinolyl)alkanoic acids IVa-e by means of LiAlH4 was used for the preparation of corresponding primary alcohols Ia-e. 6-(1,2,3,4-Tetrahydro-2-isoquinolyl)-1-hexanol (Ie) was also obtained on reduction of ester amide VII. Reduction of 2-(2-hydroxypropanoyl)-1,2,3,4-tetrahydroisoquinoline (V) with LiAlH4 gave secondary alcohol II; in the quinoline series alcohol IIIa was obtained in a similar manner by reduction of ethyl 3-(1,2,3,4-tetrahydro-1-quinolyl)propanoate (IIIb).
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
3 articles.
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