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[3+3] Cyclizations of 1,3‐Bis(silyl enol ether)s with 1,1‐Diacetylcyclopentane and 1,1‐Diacetylcyclopropane
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2003
Year
Natural Product SynthesisHeterocyclicMedicineOrganic ChemistryDomino ReactionsMs=molecular SievesChemistryHeterocycle ChemistryPharmacologyEnantioselective SynthesisDrug DiscoveryVersatile Intermediates
Domino reactions of 1,3-bis(silyl enol ether)s with 1,1-diacetylcyclopentane and 1,1-diacetylcyclopropane (see scheme) allow a new and convenient one-pot synthesis of spiro[5.4]cyclodecenones, bicyclo[4.4.0]deca-1,4-dien-3-ones, and functionalized salicylates, which are versatile intermediates for the synthesis of pharmacologically relevant natural product analogues. MS=molecular sieves. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2003/z51263_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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