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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85854
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dc.contributor.authorWarrener, R.N.-
dc.contributor.authorTan, R.Y.S.-
dc.contributor.authorRussell, R.A.-
dc.date.issued1979-
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.issn0040-4039-
dc.identifier.issn1873-3581-
dc.identifier.urihttp://hdl.handle.net/2440/85854-
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.language.isoen-
dc.publisherPergamon Press-
dc.rights© Pergamon Press Ltd. 1979.-
dc.source.urihttp://dx.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-
dc.identifier.doi10.1016/S0040-4039(01)86459-5-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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