| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5226230 | Tetrahedron | 2009 | 7 Pages |
Abstract
(â)-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 were induced through an intermolecular and an intramolecular Pictet-Spengler reaction, respectively.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xiang Wei Liao, Wei Liu, Wen Fang Dong, Bao He Guan, Shi Zhi Chen, Zhan Zhu Liu,