Synthesis of β-Amino alcohols via the reduction of lactamides derived from Ethyl (2S)-Lactate with Borane-Methyl Sulfide

Synthesis of β-Amino alcohols via the reduction of lactamides derived from Ethyl (2S)-Lactate with Borane-Methyl Sulfide
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用甲硫硼烷还原 (2S)-乳酸乙酯衍生的乳酰胺合成 β-氨基醇

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发表时间:
2009
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通讯作者:
D. H. Grayson
D. H. Grayson
中科院分区:
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文献类型:
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作者:
F. Lewis;M. Eichler;D. H. Grayson

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(2S)-乳酸乙酯与各种胺的反应得到乳酰胺,在三氟化硼醚合物存在下用甲硼烷-甲硫醚还原,以良好的收率生成对映体纯的 β-氨基醇。
Reactions of ethyl (2S)-lactate with various amines affords lactamides that are reduced with borane-methyl sulfide in the presence of boron trifluoride etherate to generate enantiomerically pure β-amino alcohols in good yield.