Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1257283 | Chinese Chemical Letters | 2013 | 4 Pages |
Abstract
In this paper, we report a total synthesis of a naturally occurring pyrrolo[2,3-d]pyrimidine nucleoside, mycalisine A. Our synthetic strategy uses d-xylose as the starting material and Vorbrüggen glycosylation as the key step. Mycalisine A was synthesized in 11 steps with a 15% overall yield.
Graphical abstractIn this paper, we report a total synthesis of a naturally occurring pyrrolo[2,3-d]pyrimidine nucleoside, mycalisine A. Our synthetic strategy uses d-xylose as the starting material and Vorbrüggen glycosylation as the key step.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Yan-Hui Dou, Hai-Xin Ding, Ru-Chun Yang, Wei Li, Qiang Xiao,