Odorless and Practical Thioacetalization Reagent: Methyl 2-(1,3-Dithian-2-ylidene)-3-oxobutanoate
Author:
Publisher
Wiley
Subject
General Chemistry
Reference44 articles.
1. Protecting Groups, Thieme, Stuttgart, 1994.
2. ; Protective Groups in Organic Synthesis, 3rd Ed., John Wiley and Sons, New York, 2004.
3. Methods of Reactivity Umpolung
4. Umpolung of the Reactivity of Carbonyl Compounds Through Sulfur-Containing Reagents
5. Dithioacetals as an Entry to Titanium-Alkylidene Chemistry: A New and Efficient Carbonyl Olefination
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1. Protection for the Carbonyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
2. An Efficient and Odorless Synthesis of Thioethers Using 2-[Bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides as Thiol Equivalents;Chinese Journal of Chemistry;2011-12-23
3. Solvent-free Thia-Michael Addition Reactions Using 3-[Bis(alkylthio)methylene]pentane-2,4-diones as Efficient and Odorless Thiol Equivalents;Chinese Journal of Chemistry;2008-08
4. 1,3-Dioxins, Oxathiins, Dithiins, and their Benzo Derivatives;Comprehensive Heterocyclic Chemistry III;2008
5. Odorless and Practical Thioacetalization Reagent: Methyl 2-(1,3-Dithian-2-ylidene)-3-oxobutanoate.;ChemInform;2005-12-27
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