The application of ¹³C-N.M.R. spectroscopy to the determination of the stereochemistry of Diels-Alder adducts

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dc.contributor.authorTan, R.Y.S.
dc.contributor.authorRussell, R.A.
dc.contributor.authorWarrener, R.N.
dc.date.issued1979
dc.description.abstractLong-range (³J) ¹³C-H coupling is a reliable probe to evaluate the stereochemistry of cycloaddition products. The method is best applied to carbonyl containing adducts but not restricted to them. Several structures have been revised and new ones evaluated.
dc.description.statementofresponsibilityRichard Y.S. Tan, Richard A. Russell, Ronald N. Warrener
dc.identifier.citationTetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1979; 20(52):5031-5034
dc.identifier.doi10.1016/S0040-4039(01)86781-2
dc.identifier.issn0040-4039
dc.identifier.issn1873-3581
dc.identifier.urihttp://hdl.handle.net/2440/85852
dc.language.isoen
dc.publisherPergamon Press
dc.rights©Pergamon Press Ltd. 1979
dc.source.urihttps://doi.org/10.1016/s0040-4039(01)86781-2
dc.titleThe application of ¹³C-N.M.R. spectroscopy to the determination of the stereochemistry of Diels-Alder adducts
dc.title.alternativeThe application of (13)C-N.M.R. spectroscopy to the determination of the stereochemistry of Diels-Alder adducts
dc.typeJournal article
pubs.publication-statusPublished

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