Cycloaddition reaction of vinylketene dithioacetals with generated -benzoquinones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. α-Oxo ketene dithioacetals and related compounds: versatile three-carbon synthons
2. α-Oxoketene-S,S-, N,S- and N,N-acetals: Versatile intermediates in organic synthesis
3. Studies on diels-alder cycloadditions of vinylketene dithioacetals
4. Cycloaddition reactions of vinylketene thioacetals
5. Conjugate and Diels-Alder reactions of an activated allylidenedithiane
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2. Experimental and Theoretical Justification for the Regiospecific Cycloaddition of Levopimaric Acid to 2-Acetyl- or 2-(Methoxycarbonyl)-1,4-Benzoquinone;Chemistry of Natural Compounds;2015-11
3. ChemInform Abstract: Cycloaddition Reaction of Vinylketene Dithioacetals with in situ Generated p-Benzoquinones.;ChemInform;2010-08-17
4. Functions Incorporating Two Chalcogens Other Than Oxygen;Comprehensive Organic Functional Group Transformations II;2005
5. Collision-induced dissociation of MCl+ adducts (M?=?Mg, Mn, Zn, Co, Ni and Cu) and Cu+ and Ag+ adducts of dithioalkyl ketene acetals;Rapid Communications in Mass Spectrometry;2001
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