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Diels-Alder Reaction of Cyclopenta-1,3-diene and Anthracene to bis-Fumarates Derived from Menthol Analogues

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dc.abstract.enDue to steric interactions of the overly bulky substituted 8‐position, the classic 8‐Ph‐menthol (‐)‐1 d is not the optimal chiral auxiliary for the asymmetric Diels‐Alder reaction of its bis fumarate (‐)‐2 d to dienes such as cyclopenta‐1,3‐diene 3 b, or anthracene 3 c. This prosthetic group (‐)‐1 d could efficiently be replaced by an intermediate smaller analog (‐)‐1 e, readily prepared in a single step by cyclopropanation of isopulegol (‐)‐1 b. This latter auxiliary, resulting from the industrial technology developed by Takasago for menthol (‐)‐1 a, does not necessitate the stereoselective ketone reduction and chromatographic separation of the usual Michael adducts, derived from (+)‐pulegone. This chiral auxiliary (‐)‐1 e, never used as an asymmetric Diels‐Alder promoter, is much more selective than menthol (‐)‐1 a itself, under uncatalyzed conditions, and is also more stable than the polymerizable isopulegyl derived dienophiles, under Lewis acid mediated conditions. This prosthetic group thus readily allows large scale operations in both accessible enantiomeric series.
dc.affiliationUniwersytet Warszawski
dc.contributor.authorChapuis, Christian
dc.contributor.authorPiątek, Anna Maria
dc.date.accessioned2024-01-24T21:48:29Z
dc.date.available2024-01-24T21:48:29Z
dc.date.issued2019
dc.description.financeNie dotyczy
dc.description.number8
dc.description.volume4
dc.identifier.doi10.1002/SLCT.201803003
dc.identifier.urihttps://repozytorium.uw.edu.pl//handle/item/104821
dc.identifier.weblinkhttps://doi.org/10.1002/slct.201803003
dc.languageeng
dc.relation.ispartofChemistrySelect
dc.relation.pages2288-2292
dc.rightsClosedAccess
dc.sciencecloudnosend
dc.subject.enAsymmetric
dc.subject.enDiels-Alder
dc.subject.enisopulegol
dc.subject.enmenthol
dc.subject.enpulegol
dc.titleDiels-Alder Reaction of Cyclopenta-1,3-diene and Anthracene to bis-Fumarates Derived from Menthol Analogues
dc.typeJournalArticle
dspace.entity.typePublication