期刊
ORGANIC LETTERS
卷 13, 期 5, 页码 1040-1043出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol1030926
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资金
- EPSRC
- Engineering and Physical Sciences Research Council [EP/E010598/1, EP/G013470/1] Funding Source: researchfish
- EPSRC [EP/G013470/1, EP/E010598/1] Funding Source: UKRI
Chiral alpha-alkyl,alpha-vinyl amino acids (quaternary vinyl glycine derivatives) are prepared with high levels of enantiomeric purity by [2,3)-sigmatropic rearrangement of allylic selenimides. The required trisubstituted allylic selenides are prepared by an organocatalytic alpha-selenenylation of aldehydes followed by Horner-Wadsworth-Emmons (HWE) olefination. Both (E)-and (Z)-geometrical isomers are available giving access to both enantiomers of the desired products.
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