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08:41
Identification of Fatty Acids in Bacillus cereus
Published on: December 5, 2016
Spirastrellolide B reveals the absolute configuration of the spirastrellolide macrolide core
Kaoru Warabi1, David E Williams, Brian O Patrick
1Department of Chemistry and Earth and Ocean Sciences, University of British Columbia, Vancouver, BC, Canada.
Journal of the American Chemical Society
|January 18, 2007
Abstract
No abstract available in PubMed .
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Different notations are used to represent the three-dimensional structure of molecules on two-dimensional surfaces. One of the most commonly used representations is the dash-wedge formula. The dashed wedges, solid wedges, and the plane lines indicate the groups situated behind the plane, coming out of the plane, and in the plane, respectively.
The organic molecules rotate across the single bonds leading to numerous temporary three-dimensional structures of varying energy known as conformers.
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Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied first.
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The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.

