Article 2022 · 3 citations

Efficient synthesis of aziridinecyclooctanediol and 3-aminocyclooctanetriol

Abstract

Cyclooctene endoperoxide was used as the key compound for the synthesis of aziridinecyclooctanediol and 3-aminocyclo-octanetriol. Reduction of the cyclooctene endoperoxide, prepared by photooxygenation of cis,cis-1,3-cyclooctadiene, with zinc gave a cyclooctenediol and then benzylation of the hydroxy group yielded dibenzylated cyclooctene. Oxidation of the latter compound by OsO4/NMO followed by mesylation of the hydroxy group provided bis(benzyloxy)cyclooctane-1,2-diyl dimethanesulfonate. Reaction of the bis(benzyloxy)cyclooctane-1,2-diyl dimethanesulfonate with NaN3 gave 2-azido-3,8-bis(benzyloxy)cyclooctyl methanesulfonate. Reduction of the azide group and debenzylation to give an amine provided the new 3-aminocyclooctanetriol. Treatment of the 2-azido-3,8-bis(benzyloxy)cyclooctyl methanesulfonate with Zn/NH4Cl and debenzylation resulted in the target aziridinecyclooctanediol.

Keywords

aminocyclitols aminocyclooctanetriol azides aziridines aziridinecyclooctanediol STEREOSPECIFIC SYNTHESIS DL-PROTO AMINOCYCLITOLS AZIRIDINATION DERIVATIVES QUERCITOL CONCISE ANALOGS

WoS Categories

Chemistry, Organic

Sustainable Development Goals

Good Health and Well-being

Citation

Journal: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
Year: 2022
Volume: 18
Pages: 1539-1543
ISSN: 1860-5397
DOI: 10.3762/bjoc.18.163
WoS UID: WOS:000885349300001

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