A Catalytic Enantioselective Route to Hydroxy-Substituted Quaternary Carbon Centers: Resolution of Tertiary Aldols with a Catalytic Antibody
- 28 July 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (32) , 7283-7291
- https://doi.org/10.1021/ja991507g
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- A method for collection, long-term storage, and bioassay of labile volatile chemosignalsJournal of Chemical Ecology, 1996
- Enantioselective Synthesis of Tertiary Homoallylic Alcohols via Diastereoselective Addition of Allylsilanes to KetonesJournal of the American Chemical Society, 1995
- Enantioselective Aldol Reaction of tert‐Butyl Acetate using Titanium‐Carbohydrate ComplexesAngewandte Chemie International Edition in English, 1989
- Structural elucidation of a novel deoxynivalenol analogThe Journal of Organic Chemistry, 1987
- Hydroboration. 75. Directive effects in the hydroboration of vinyl and propenyl heterocycles with representative hydroborating agentsThe Journal of Organic Chemistry, 1986
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- Magnetic resonance spectroscopy on carbon-13 labeled uracil in transfer ribonucleic acidJournal of the American Chemical Society, 1976
- Preparation of chiral compounds with high optical purity by irradiation with circularly polarized light, a model reaction for the prebiotic generation of optical activityJournal of the American Chemical Society, 1974
- The Stereochemistry of the Ivanov and Reformatsky Reactions. IJournal of the American Chemical Society, 1957
- β-HYDROXY-β-METHYL-δ-VALEROLACTONE (DIVALONIC ACID), A NEW BIOLOGICAL FACTORJournal of the American Chemical Society, 1956