Homochiral Perfluoroalkyl-Group-Substituted Secondary Alcohols Through Stereoselective Reduction of Perfluoroalkyl 1-(p-Tolylsulfinyl)alkyl Ketones
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1988-27764.pdf
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Highly diastereoselective methylene transfer from diazomethane to the carbonyl of β-keto sulfoxides. A general approach to synthetically versatile fluorine-containing chiral building blocks;Tetrahedron;1998-09
2. Synthesis of selectively fluorinated molecules from dimethylsulfoxide, fluoroacetic acid esters and diazomethane;Journal of Fluorine Chemistry;1998-08
3. Remarkable effect of lithium bromide in the enantioselective protonation with α-sulfinyl alcohols;Tetrahedron Letters;1998-05
4. Trifluoromethyl vs. methyl ability to direct enantioselection in microbial reduction of carbonyl substrates.;Tetrahedron;1998-03
5. Highly enantiofacial protonation of prochiral lithium enolates with chiral β-hydroxy sulfoxides;Tetrahedron Letters;1997-09
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