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Chemical shift assignment of geminal protons in 3,7-diazabicyclo [3.3.1]nonanes: An unexpected deviation from the axial/equatorial chemical shift order
Uppsala University.
Uppsala University.
Uppsala University.
1997 (English)Other (Other academic)
Abstract [en]

The chemical shift order of axial and equatorial methylene protons in 1,5-disubstituted 3,7-diazabicyclo [3.3.1]nonan-9-ones may be altered by substituents in the 1,5-positions, but the corresponding alcohols behave differently. Unambiguous signal assign

Place, publisher, year, edition, pages
JOHN WILEY & SONS LTD , 1997. Vol. 35, no 1, 13-20 p.
Keyword [en]
NMR; H-1 NMR; C-13 NMR; 3;7-diazabicyclo[3.3.1]nonane; heteronuclear Overhauser effect; HSBC; 2D heteronuclear correlation; MOLECULAR-STRUCTURE; PENTAARYL-1;3-DIAZAADAMANTANES; STEREOCHEMISTRY; CONFORMATION; SPECTROSCOPY; DERIVATIVES; COMPLEXES; RESONAN
URN: urn:nbn:se:uu:diva-82602DOI: 10.1002/(SICI)1097-458X(199701)OAI: oai:DiVA.org:uu-82602DiVA: diva2:110508
Addresses: Gogoll A, UNIV UPPSALA, DEPT ORGAN CHEM, BOX 531, S-75121 UPPSALA, SWEDEN.Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-08

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Gogoll, AdolfGrennberg, Helena
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