A Simple Method for Generation of Thiocarbonyl Ylides and Their Regioselective 1,3-Cycloadditions
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference9 articles.
1. Thiocarbonyl ylides. VI. New generation of thiocarbonyl ylides from organosilicon compounds containing sulfur and their 1,3-cycloadditions.
2. Cycloaddition with utilization of chemical characteristics of silicon atom.
3. Ylides by the desilylation of .alpha.-silyl onium salts
4. New generation of thiocarbonyl ylide and its 1,3-cycloaddition leading to tetrahydrothiophene derivatives
5. Effect of a Silyl Group on the Regio- and Stereoselectivity in 1,3-Dipolar Cycloaddition
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1. Sila-Pummerer Rearrangement of Cyclic Sulfoxides: Computational Study of the Mechanism;Journal of the American Chemical Society;2004-08-26
2. Conformational behavior of 3,3-dimethyl-3-silathiane 1-oxide and its diastereomeric 2-methyl derivatives;Journal of Sulfur Chemistry;2004-02
3. A Computational Study of the Cycloaddition of Thiobenzophenone S-Methylide to Thiobenzophenone;Journal of the American Chemical Society;2003-11-01
4. Reactions of ThiobenzophenoneS-Methylide with Thiocarbonyl Compounds;European Journal of Organic Chemistry;2000-05
5. Enantiomerically Pure trans-3,4-Disubstituted Tetrahydrothiophenes from Diastereoselective Thiocarbonyl Ylide Addition to Chiral α,β-Unsaturated Amides;Organic Letters;1999-10-10
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