Zur Stereoselektivität der nucleophilen Addition an die sterisch ungehinderten Ketone 2‐Phenyl‐1,3‐dioxan‐5‐on und 2‐Phenyl‐1,3‐dithian‐5‐on
- 1 October 1978
- journal article
- organische chemie
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 111 (10) , 3442-3459
- https://doi.org/10.1002/cber.19781111018
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Conformational control. An important factor in the stereoselective reduction of ketones by bulky hydride reagentsThe Journal of Organic Chemistry, 1977
- Simulation and evaluation of chemical synthesis. Congestion: a conformation-dependent function of steric environment at a reaction center. Application with torsional terms to stereoselectivity of nucleophilic additions to ketonesJournal of the American Chemical Society, 1976
- Stereochemistry of organometallic compound addition to ketonesChemical Reviews, 1975
- Mechanisms of Grignard reagent addition to ketonesAccounts of Chemical Research, 1974
- Ring inversion in cyclohexanoneJournal of the American Chemical Society, 1973
- Reduction with metal hydrides—XIXTetrahedron, 1970
- Internal reactions in the Grignard‐complex containing compounds with alkoxy‐groups: Part II. Cyclic acetalsRecueil des Travaux Chimiques des Pays-Bas, 1963
- Conformational Analysis. III. Epimerization Equilibria of Alkylcyclohexanols1Journal of the American Chemical Society, 1957
- The Stereochemistry of Hydride ReductionsJournal of the American Chemical Society, 1956
- Über die αγ‐BenzylidenglyceroleRecueil des Travaux Chimiques des Pays-Bas, 1942