ISSN:
0030-4921
Keywords:
Chemistry
;
Analytical Chemistry and Spectroscopy
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Standard values of vicinal coupling constants are proposed in order to assign relative configuratations and analyse the conformational distribution of acyclic chiral carbinols and hydrocarbons. Thus, the assignment of relative configurations has been achieved for the diastereomeric carbinols, (2R4R, 2S4S)- and (2R4S, 2S4R)-5,5-dimethyl-4-phenyl-2-hexanol and (1R3R, 1S3S)- and (1R3S, 1S3R)-1-mesityl-4,4-dimethyl-3-phenyl-1-pentanol, through the analysis of the respective vicinal coupling constants and the corresponding conformational distribution. The analysis of the vicinal coupling constants allows the establishment of the monoconformational character of the (2R4S, 2S4R) diastereomer in the first case and the (1R3R, 1S3S) diastereomer in the second case.
Additional Material:
1 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/mrc.1270180411
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