3-(Alkylthio)-1,2-bis(siloxy)-3-butenes as efficient chirality transferred building blocks
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. A novel transformation involving selective formation and cleavage of carbon-carbon bonds
2. Acid-Promoted Reactions of Schiff’s Bases with Ketene Dithioacetal, Vinyl Sulfides, and 1,2-Propadienyl Sulfides
3. Reactions of 1,2-Propadienyl Sulfides with Aldehydes and Acetals Catalyzed by BF3·OEt2
4. A cross-aldol type reaction of alkenyl sulfide with trimethylsilyl enol ether.
5. A Convenient Method for the Transformation of Alkenyl Sulfides to 2-(Phenylthio)alkanenitriles, Homoallyl Sulfides, and Thioacetals
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1. γ-Substituted Butanolides from Cyclopropane Hemimalonates: An Expedient Synthesis of Natural (R)-Dodecan-4-olide;Organic Letters;2013-09-05
2. Enantioselective transesterification of (±)-1-phenylundecan-3-ol catalyzed by the lipase from Burkholderia cepacia;Russian Chemical Bulletin;2013-09
3. Alkylaluminum Chlorides;Fieser and Fieser's Reagents for Organic Synthesis;2013-04-26
4. Alkylaluminum Chlorides;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15
5. ChemInform Abstract: 3-(Alkylthio)-1,2-Bis(siloxy)-3-butenes as Efficient Chirality Transferred Building Blocks.;ChemInform;2010-08-18
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