The stereochemistry of the adducts derived from the Diels-Alder addition of cyclobutenes and cyclopentadienones: a caveat on some existing PMR methods for the assignment of stereochemistry

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dc.contributor.authorWarrener, R.N.
dc.contributor.authorTan, R.Y.S.
dc.contributor.authorRussell, R.A.
dc.date.issued1979
dc.description.abstractThe stereochemistry of the adducts formed from the cycloaddition of tetracyclone, phencyclone and 2-methyl-3,4,5-triphenylcyclopenta-2,4-dienone with cis-3,4-dichlorocyclobutene (in one case with 3-chloro-4-methoxycyclobutene) has been evaluated in a rigorous fashion. This allows a firmly-based caveat to be issued regarding the p.m.r. probe for stereochemical evaluation of tetracyclone adducts recently proposed by Coxon and Battiste.
dc.description.statementofresponsibilityRonald N. Warrener, Richard Y.S. Tan, Richard A. Russell
dc.identifier.citationTetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1979; 20(31):2943-2946
dc.identifier.doi10.1016/S0040-4039(01)86459-5
dc.identifier.issn0040-4039
dc.identifier.issn1873-3581
dc.identifier.urihttp://hdl.handle.net/2440/85854
dc.language.isoen
dc.publisherPergamon Press
dc.rights© Pergamon Press Ltd. 1979.
dc.source.urihttps://doi.org/10.1016/s0040-4039(01)86459-5
dc.titleThe stereochemistry of the adducts derived from the Diels-Alder addition of cyclobutenes and cyclopentadienones: a caveat on some existing PMR methods for the assignment of stereochemistry
dc.typeJournal article
pubs.publication-statusPublished

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