Microwave-induced organic reaction enhancement chemistry.4 convenient synthesis of enantiopure α-hydroxy-β-lactams1
暂无分享，去创建一个
B. Banik | M. S. Manhas | K. Barakat | Z. Kaluza | A. Rosé
[1] V. S. Raju,et al. Microwave-induced organic reaction enhancement chemistry. 2. Simplified techniques , 1991 .
[2] Joseph L. Phillips,et al. SYNTHESIS OF 2,3-O-ISOPROPYLIDENE-D-GLYCERALDEHYDE IN HIGH CHEMICAL AND OPTICAL PURITY : OBSERVATIONS ON THE DEVELOPMENT OF A PRACTICAL BULK PROCESS , 1991 .
[3] V. Hegde,et al. Studies on lactams. 81. Enantiospecific synthesis and absolute configuration of substituted .beta.-lactams from D-glyceraldehyde acetonide , 1988 .
[4] S. S. Bari,et al. Enantiospecific synthesis of β-lactams via cycloaddition , 1985 .
[5] G. Schmid,et al. An enantioselective β-lactam synthesis starting from L-(S)-glyceraldehyde acetonide , 1983 .
[6] B. Belleau,et al. A highly asymmetric synthesis of the O-2-isocephem class of β-lactam antibiotics , 1980 .
[7] E. Baer,et al. STUDIES ON ACETONE-GLYCERALDEHYDE IV. PREPARATION OF d(+)-ACETONE GLYCEROL , 1939 .