1177255-26-3Relevant academic research and scientific papers
Total synthesis of (-)-MY 336a from L-tyrosine
Liao, Xiang Wei,Dong, Wen Fang,Liu, Wei,Guan, Bao He,Liu, Zhan Zhu
experimental part, p. 50 - 53 (2010/05/03)
(Chemical Equation Presented) Using L-tyrosine as a chiral starting material, we developed an efficient synthetic route to (-)-MY 336a. A key step in the sequence is a highly regio- and diastereoselective intermolecular Pictet-Spengler cyclization reaction between amino alcohol and benzyloxyacetaldehyde.
Total synthesis of (-)-renieramycin G from l-tyrosine
Liao, Xiang Wei,Liu, Wei,Dong, Wen Fang,Guan, Bao He,Chen, Shi Zhi,Liu, Zhan Zhu
supporting information; experimental part, p. 5709 - 5715 (2009/12/04)
(-)-Renieramycin G was synthesized in 21 steps for the longest linear sequences employing l-tyrosine methyl ester as the chiral starting material in 8.5% overall yield. Two of the four chiral centers came from l-tyrosine methyl ester, and the other two we
