In contrast to the reported reaction between trans-l-aminotetralin-2-01 and formaldehyde, which gives r-6a, c-9a,t-15a,t-18a-5,6,6a,9a,14,15,15a,18a-o~ahy~o-9,18-me~~odinaphtho [ 1,2-d: 1',2'-i] [1,6,3,8]dioxadiazecine, an examination of the 6 4.0-5.0 region of the 'H NMR spectra of the products of
Compounds with bridgehead nitrogen. Part 47. The reaction between trans-1-aminobenzocycloalkan-2-ols and formaldehyde
β Scribed by Barkworth, Peter M. R.; Crabb, Trevor A.; Robinson, Paul
- Book ID
- 118191504
- Publisher
- Royal Society of Chemistry
- Year
- 1983
- Weight
- 441 KB
- Category
- Article
- ISSN
- 1472-7781
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huns-l-N-Alkylaminotetralin-2-ols condense with formaldehyde to form the expected truns-(H3a, H-9b)-Nalkyl-1,2,3a,4,5,9b-hexahydronaphtho[l,2-d][l,3]oxazoles. On allowing solutions of these compounds in deuteriochloroform to stand for several hours a mixture of the original oxazole, together with a
## Abstract The effect of 6βsubstitution on the conformational equilibria of the perhydrodipyrido[1,2β__c__:2β²,1β²β__e__]imidazoles has been investigated. __r__β6H,__t__β11a,__t__β11bβ6β__p__βNitrophenylperhydrodipyrido[1,2β__c__:2β²,1β²β__e__]imidazole was found to exist as a pair of enantiomeric non