Complete 1,3-asymmetric induction in the reactions of allenylboronic acid with β-hydroxy ketones
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (10) , 1175-1178
- https://doi.org/10.1016/s0040-4039(00)84209-4
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Utilization of the chiral synthon, methyl 3-O-benzyl-2,4,6-trideoxy-6-iodo-α-D-Tetrahedron Letters, 1985
- Concerning the role of Lewis acids in chelation controlled addition to chiral alkoxy aldehydesTetrahedron Letters, 1984
- Stereochemistry of the sn2′ displacement of chiral 1, 3-disubstituted bromoallenes to form chiral acetylenesTetrahedron Letters, 1984
- Acyclic stereoselection. 20. High diastereofacial selectivity in the stannic chloride mediated reactions of allylsilanes with chiral α- and β-alkoxy aldehydes.Tetrahedron Letters, 1983
- A diastereoselective synthesis of 4(RS), 6(SR)-mercaptomethylmevalonolactone, a key intermediate in the preparation of a new class of inhibitors of HMG-CoA reductaseTetrahedron Letters, 1983
- 1,3-Asymmetric induction in addition reactions of chiral .beta.-alkoxy aldehydes: efficient chelation control via Lewis acidic titanium reagentsJournal of the American Chemical Society, 1983
- Chiral allenylboronic esters: a practical reagent for enantioselective carbon-carbon bond formationJournal of the American Chemical Society, 1982
- Structural modification of mevinolinThe Journal of Organic Chemistry, 1982
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981
- Chelation-controlled nucleophilic additions. 1. A highly effective system for asymmetric induction in the reaction of organometallics with α-alkoxyketones.Tetrahedron Letters, 1980