Enantioselective synthesis of (2S,3R)-3-hydroxy-3-methylproline, a novel amino acid found in polyoxypeptins.
Enantioselective synthesis of (2S,3R)-3-hydroxy-3-methylproline, a novel amino acid found in polyoxypeptins.
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(2S,3R)-3-羟基-3-甲基脯氨酸(聚氧肽素中发现的一种新型氨基酸)的对映选择性合成。
DOI:
10.1021/jo016227
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发表时间:
2002
期刊:
影响因子:
--
通讯作者:
Z. Yao
中科院分区:
文献类型:
--
作者:
Dongguang Qin;Huiyan Zha;Z. Yao
The enantioselective synthesis of (2S,3R)-3-hydroxy-3-methylproline (3) was achieved by the Sharpless AD, regioselective opening of cyclic sulfate by NaN(3) and intramolecular ring-closing reaction. The reported route has the advantage of a high overall yield and good enantiomeric purity, as well as starting from readily available chemical substrates and inexpensive reagents.