Vitesses de reduction de ceto-3 steroides par le tri-terbutoxy-hydruro aluminate de lithium
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. On the Stereochemistry of the Reduction of Cyclic Ketones with Lithium Tri-t-butoxyaluminum Hydride
2. Asymetric induction. II. On the extent of bond breaking and making in the transition states of some additions to carbonyls
3. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones
4. Torsional strain involving partial bonds. The steric course of the reaction between allyl magnesium bromide and 4-t-butyl-cyclohexanone
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1. Inductive and Resonance Effects of Substituents on π-Face Selection;Chemical Reviews;1999-05-12
2. Parabolic Relationship between the Basicity of the Nucleophile and π-Face Selection in Addition of the Substituted Acetylide Ions to Cyclohexanone and Cyclohexanethione;The Journal of Organic Chemistry;1998-01-22
3. Stereochimie—LII. Controle orbitalaire de la stereochimie des reactions—III;Tetrahedron;1980-01
4. Influnce des interactions de torsion dans la reduction des cetones par les hydrures interpretation generale du deroulement sterique de la reduction des cetones acycliques et de l'addition des organomagnesiens sur les aldehydes acycliques;Tetrahedron;1980-01
5. Influence des interactions de torsion dans les reactions d'addition sur les cyclohexanones. interpretation generale du deroulement sterique des reactions des hydrures ou des organomagnesiens sur les cyclohexanones;Tetrahedron;1980
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