Novel Stereoselective Syntheses of (+)-Streptol and (−)-1-epi-Streptol Starting from Naturally Abundant (−)-Shikimic Acid

[Image: see text] Novel highly stereoselective syntheses of (+)-streptol and (−)-1-epi-streptol starting from naturally abundant (−)-shikimic acid were described in this article. (−)-Shikimic acid was first converted to the common key intermediate by 11 steps in 40% yield. It was then converted to (...

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Detalles Bibliográficos
Autores principales: Zhu, Xing-Liang, Luo, Yong-Qiang, Wang, Lei, Huang, Yong-Kang, He, Yun-Gang, Xie, Wen-Jing, Liu, Shi-Ling, Shi, Xiao-Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264934/
https://www.ncbi.nlm.nih.gov/pubmed/34250367
http://dx.doi.org/10.1021/acsomega.1c02502

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264934/
https://www.ncbi.nlm.nih.gov/pubmed/34250367
http://dx.doi.org/10.1021/acsomega.1c02502

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