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Stereoselective synthesis of C5-C10 segment 3 of taurospongin A (1) has been developed successfully from L-(-)-malic acid.
Synthesis of the C5-C10 Segment of Taurospongin A
【摘 要】
：
Stereoselective synthesis of C5-C10 segment 3 of taurospongin A (1) has been developed successfully from L-(-)-malic acid.
【机 构】
：
Shanghai Institute of Materia Medica
【出 处】
：
中国化学快报（英文版）
【发表日期】
：
2004年期
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