Diastereotopic group selectivity at a prostereogenic carbon center: Synthesis of (±)-syn-4,8-dimethyldecanal
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (38) , 4561-4564
- https://doi.org/10.1016/s0040-4039(00)85003-0
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- The epoxidation of unsaturated macrolides. Stereocontrolled routes to ionophore subunitsJournal of the American Chemical Society, 1986
- Diastereotopic selectivity at prochiral carbon centers: functionalization of differentiated hydroxymethyl groups provides access to either stereoisomeric configurationJournal of the American Chemical Society, 1985
- Pheromone syntheses, LXXIII. New synthesis of (4R,8R)‐4,8‐dimethyldecanal, the aggregation pheromone of tribolium castaneum, and its (4R,8S)‐isomerEuropean Journal of Organic Chemistry, 1985
- A synthesis of talaromycin BJournal of the Chemical Society, Chemical Communications, 1984
- NOC approach to spiroketals. A total synthesis of (.+-.)-talaromycin BJournal of the American Chemical Society, 1984
- Chirality transfer in stereoselective synthesis. A highly stereoselective synthesis of optically active vitamin E side chainsThe Journal of Organic Chemistry, 1983
- 1,7-Dioxaspiro[5.5]undecanes. An excellent system for the study of stereoelectronic effects (anomeric and exo-anomeric effects) in acetalsCanadian Journal of Chemistry, 1981
- Method for catalytic dehalogenations via trialkyltin hydridesThe Journal of Organic Chemistry, 1975
- Reactions of lithium diorganocuprates(I) with tosylates. I. Synthetic aspectsJournal of the American Chemical Society, 1973
- Stereoisomeric Relationships of Groups in MoleculesTopics in Stereochemistry, 1967