Mediation of a primary kinetic isotope effect by asymmetric induction
Author:
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja01044a080
Cited by 7 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. A Summary of Ways to Obtain Optically Active Compounds;Asymmetric Synthesis;1983
2. Inverse kinetic isotope effect in the reduction of hindered ketones by lithium aluminum tris(tert-butoxide) and deuterium-labeled lithium aluminum tris(tert-butoxide);Journal of the American Chemical Society;1975-02
3. Reduction of phenyl trifluoromethyl ketone with halomagnesium alkoxides. Almost irreversible Meerwein-Ponndorf-Verley type system;The Journal of Organic Chemistry;1974-10
4. Alkyl metal asymmetric reduction. Part IV. Reduction of isopropyl phenyl ketone by optically active dialkylzinc compounds: dependence of stereoselectivity on the distance of the chiral centre from the metal atom;Journal of the Chemical Society, Perkin Transactions 1;1974
5. Alkyl metal asymmetric reduction. III. Stereochemistry of alkyl phenyl ketone reductions by chiral organoaluminum compounds;The Journal of Organic Chemistry;1973-06
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