Highly Diastereoselective Reduction of Chiral (Ferrocenylseleno)methyl Aryl and Alkyl Ketones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/28/3/28_3_245/_pdf
Reference14 articles.
1. Asymmetric Methoxyselenenylation of Alkenes with Chiral Ferrocenylselenium Reagents
2. Synthesis of [R,S;R,S]- and [S,R;S,R]-Bis[2-[1-(dimethylamino)ethyl]ferrocenyl] Diselenides and Their Application to Asymmetric Selenoxide Elimination and [2,3]Sigmatropic Rearrangement
3. Mono-Cr(CO)3 complexes of biphenyl compounds: Cross-coupling reactions of (η6-arene)chromium complexes with arylmetals
4. Stereospecific hydroxylation of chiral allylic β-hydroxysulfoxides: Applications to the asymmetric synthesis of optically active vicinal triols
5. Reduction of .beta.-keto sulfoxides: a highly efficient asymmetric synthesis of both enantiomers of allylic alcohols
Cited by 4 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. Stereoselective Reactions of Organoselenium Reagents Including Catalysis;PATAI'S Chemistry of Functional Groups;2011-03-15
2. ChemInform Abstract: Highly Diastereoselective Reduction of Chiral (Ferrocenylseleno)methyl Aryl and Alkyl Ketones.;ChemInform;2010-06-14
3. Organoselenium Chemistry in Stereoselective Reactions;Angewandte Chemie;2000-11-03
4. Organoselenchemie in der stereoselektiven Synthese;Angewandte Chemie;2000-11-03
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