Asymmetric synthesis using a new chiral β-functionalized allylboronate derived from endo-2-phenyl-exo-2,3-bornanediol: Preparation and reactions with aldehydes
- 26 May 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (21) , 3719-3722
- https://doi.org/10.1016/s0040-4039(97)00708-9
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- A hypothesis for conformational restriction in complexes of formyl compounds with boron Lewis acids. Experimental evidence for formyl CH--O and CH--F hydrogen bondsTetrahedron Letters, 1997
- 2,3-O-(3-Pentylidene)-D-glyceraldehyde and 2,3-O-(3-Pentylidene)-L-glyceraldehyde: Convenient Glyceraldehyde Surrogates Obtained via a Novel Periodate-Based Oxdation SystemSynthesis, 1992
- Boronic Esters in Stereodirected SynthesisTetrahedron, 1989
- N,N'-dibenzyl-N,N'-ethylenetartramide: a rationally designed chiral auxiliary for the allylboration reactionJournal of the American Chemical Society, 1988
- On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcoholsThe Journal of Organic Chemistry, 1986
- Conversion of 2,3-O-isopropylidene-d-glyceraldehyde into 2-deoxy-d-erythro-pentoseCarbohydrate Research, 1983
- Diastereogenic Addition of Crotylmetal Compounds to AldehydesAngewandte Chemie International Edition in English, 1982
- Stereoselektive Synthese von Alkoholen, VI1) Asymmetrische Synthesen von 4‐Penten‐2‐ol über Allylboronsäureester chiraler GlycoleEuropean Journal of Inorganic Chemistry, 1981
- Stereoselektive Synthese von Alkoholen, VII1) Optisch aktive Homoallylalkohole durch Addition chiraler Boronsäureester an AldehydeEuropean Journal of Inorganic Chemistry, 1981
- Enantioselective Synthesis of Homoallyl Alcohols via Chiral Allylboronic EstersAngewandte Chemie International Edition in English, 1978