Author:
Lewis PH,Middleton S,Rosser MJ,Stock LE
Abstract
When treated with nitrous
acid, the trans-fused amino alcohol (3) undergoes 'normal' stereospecific
deamination to give the trans-fused octahydroindene-1-carbaldehyde (20) in
contrast with the reported 'abnormal' behaviour of the related amino sterol
(1).
Cited by
3 articles.
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1. Bicyclo[4.4.0]decanes;Stereochemical Analysis of Alicyclic Compounds by C-13 NMR Spectroscopy;1987
2. Bicyclo[4.3.0]nonanes;Stereochemical Analysis of Alicyclic Compounds by C-13 NMR Spectroscopy;1987
3. ChemInform Abstract: STEREOCHEMICAL STUDIES. VII. SYNTHESIS AND DEAMINATION OF STEREOISOMERIC 2-AMINODECAHYDRONAPHTHALEN-1-OLS;Chemischer Informationsdienst;1980-09-30