Publication | Closed Access
Stereochemical aspects of proton chemical shifts. III—Configurational assignments in pentacyclic systems without recourse to a karplus equation
95
Citations
26
References
1975
Year
EngineeringChemical TransformationBiochemistryKarplus EquationNatural SciencesChemical Shift CriteriaProton TransferStereochemical AspectsOrganic ChemistryPseudorotational FrameworksMathematical ChemistryComputational ChemistryChemistryUnambiguous Structural ElucidationsMolecular ChemistryProton Chemical ShiftsBiophysicsLinear Chain Compound
Abstract It is shown that in contrast to the use of coupling constants, chemical shift criteria may lead to unambiguous structural elucidations in pseudorotational frameworks (pentacycles, heptacycles, etc.).
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