1-Benzyloxy-3-(p-tolylsulfonyl)propene as an acrolein β-anion equivalent. Synthesis of 4-substituted 2-butenolides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Stereoselective synthesis of 3-(phenylsulphonyl)-2,5 disubstituted tetrahydrofurans via 5-endo-trig ring-closure reactions
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3. (E)-1-Bromo-3,3-diethoxy-1-propene (diethyl acetal of 3-bromoacrolein). A versatile synthon for the synthesis of furans, butenolides, and (Z)-allyl alcohols
4. DIANIONS OFN-MONOSUBSTITUTED-3-(PHENYLSULFONYL)PROPANAMIDES. CONVENIENT REAGENTS FOR THE SYNTHESIS OF 5-ALKYL-2(5H)-FURANONES
5. Synthesis and reactivity of lithiated γ-functionalised ketene dithioacetals. Generation of a flexible β-lithioacrylate equivalent
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3. ChemInform Abstract: 1-Benzyloxy-3-(p-tolylsulfonyl)propene as an Acrolein β-Anion Equivalent. Synthesis of 4-Substituted 2-Butenolides.;ChemInform;2010-08-20
4. Evolving Organic Synthesis Fostered by the Pluripotent Phenylsulfone Moiety;Chemical Reviews;2009-05-13
5. γ-p-Toluenesulfonyl-α,β-epoxysilane: A New and Practical Acrolein β-Anion Equivalent;Organic Letters;2004-11-23
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