95727-08-5Relevant academic research and scientific papers
Synthesis of an isomer of the renieramycin skeleton from L -tyrosine
Liu, Wei,Dong, Wen Fang,Liao, Xiang Wei,Guan, Bao He,Liu, Zhan Zhu
, p. 414 - 418 (2011/06/20)
A new approach that tried to obviate the use of bromine protection groups was studied to synthesize (-)-renieramycin G from L-tyrosine. It was found that the first intermolecular Pictet-Spengler reaction proceeded successfully to give the correct tetrahyd
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.
