B-Amino acids2) are of great current interest because of their naturally occurring as the component of biologically active peptide antibiotics and also their structual relationship to the B-lactam, one of the most biologically important functional groups. We wish to describe here the catalytic asym
โฆ LIBER โฆ
Asymmetric synthesis with amino acid II asymmetric synthesis of optically active 4,4-disubstituted-cyclohexenone
โ Scribed by Shun-ichi Yamada; Genji Otani
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 228 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
In an earlier communloatlon 1) , aaymmetrlc alkylatlon of cyclohexanone enamine wae described.
Thle paper deale with an extenelon of thle reaction to the aldehyde enamlne. mamine alkylatlon was devleed by stork and hle co-workers 8)
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