ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES

KNEER G, Mattay J (1992)
Tetrahedron Letters 33(52): 8051-8054.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Abstract / Bemerkung
Moderate facial selectivities are observed in additions of alkyl radicals to the chiral (c,d) olefin (2S)-2-tert-butyl-5-ethoxycarbonylmethylene-1,3-dioxolane-4-one 1. The following hydrogen abstraction from tributylstannane proceeds with excellent asymmetric stereocontrol, leading to two of four possible diastereoisomers with high diastereomeric excesses. Additions of chiral radicals obtained from (2R,5R)-5-alkyl-5-bromo-1,3-dioxolane-4-ones to ethyl acrylate show high asymmetric 1,3-induction.
Erscheinungsjahr
1992
Zeitschriftentitel
Tetrahedron Letters
Band
33
Ausgabe
52
Seite(n)
8051-8054
ISSN
0040-4039
Page URI
https://pub.uni-bielefeld.de/record/2402741

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KNEER G, Mattay J. ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES. Tetrahedron Letters. 1992;33(52):8051-8054.
KNEER, G., & Mattay, J. (1992). ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES. Tetrahedron Letters, 33(52), 8051-8054. doi:10.1016/S0040-4039(00)74714-9
KNEER, G., and Mattay, J. (1992). ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES. Tetrahedron Letters 33, 8051-8054.
KNEER, G., & Mattay, J., 1992. ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES. Tetrahedron Letters, 33(52), p 8051-8054.
G. KNEER and J. Mattay, “ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES”, Tetrahedron Letters, vol. 33, 1992, pp. 8051-8054.
KNEER, G., Mattay, J.: ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES. Tetrahedron Letters. 33, 8051-8054 (1992).
KNEER, G, and Mattay, Jochen. “ASYMMETRIC RADICAL ADDITIONS USING CHIRAL 1,3-DIOXOLANE-4-ONES”. Tetrahedron Letters 33.52 (1992): 8051-8054.