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1982•Collection of Czechoslovak Chemical CommunicationsRequires access

Hydroboration of N-allyl derivatives of pyrrolidine, piperidine, hexahydroazepine and morpholine

M. Ferles, Stanislav Kafka

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Abstract

Heating of allyl derivatives I with triethylamine-borane gave spirocyclical amine-boranes II, which were hydrolysed with hydrochloric acid to hydrochlorides of aminoboronic acids, III. Oxidation of these hydrochlorides produced amino alcohols IV.

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What this paper is about

Heating of allyl derivatives I with triethylamine-borane gave spirocyclical amine-boranes II, which were hydrolysed with hydrochloric acid to hydrochlorides of aminoboronic acids, III. Oxidation of these hydrochlorides produced amino alcohols IV.

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Available abstract

Heating of allyl derivatives I with triethylamine-borane gave spirocyclical amine-boranes II, which were hydrolysed with hydrochloric acid to hydrochlorides of aminoboronic acids, III. Oxidation of these hydrochlorides produced amino alcohols IV.

Key concepts: Chemistry, Pyrrolidine, Morpholine, Piperidine, Triethylamine, Hydroboration, Borane, Boranes

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Hydroboration of N-allyl derivatives of pyrrolidine, piperidine, hexahydroazepine and morpholine — Research Paper | ScholarLens