NMR and X-ray structural study of saturated ( p-chlorophenyl)pyrrolo[1,2-a][3,1]benzoxazin-1-ones prepared from aroylisobutyric acid and cyclic amino alcohols. High energy barriers for hindered rotation of bridgehead phenyl groups
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1999/P2/A905445F
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1. Unexpected isomerization of new naphth[1,3]oxazino[2,3-a]isoquinolines in solution, studied by dynamic NMR and supported by theoretical DFT computations;Tetrahedron;2013-09
2. Diastereoselective Synthesis of Bicyclic γ-Lactams via Ring Expansion of Monocyclic β-Lactams;The Journal of Organic Chemistry;2009-01-26
3. Bicyclic 5-6 Systems with One Bridgehead (Ring Junction) Nitrogen Atom: One Extra Heteroatom 0:1;Comprehensive Heterocyclic Chemistry III;2008
4. Reactions of Levulinic Acid with Norbornane/ene Amino Acids and Diamines;European Journal of Organic Chemistry;2004-03
5. Structures of Saturated 5H-Pyrrolo[1,2-a][3,1]benzoxazin-1(2H)-ones Prepared from 4-Oxopentanoic Acid and Cyclic Amino Alcohols;European Journal of Organic Chemistry;2003-05
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