Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/15916
Title: Synthesis of the macrocyclic core of rhizopodin
Authors: Song, L
Liu, J
Gui, H
Hui, C
Zhou, J
Guo, Y
Zhang, P
Xu, Z
Ye, T 
Keywords: Antitumor agents
Asymmetric synthesis
Macrocycles
Natural products
Polyketides
Issue Date: 2013
Publisher: Wiley-V C H Verlag Gmbh
Source: Chemistry - an Asian journal, 2013, v. 8, no. 12, p. 2955-2959 How to cite?
Journal: Chemistry - An Asian Journal 
Abstract: Rhizing star: A stereoselective synthesis of the fully functionalized macrocyclic core of rhizopodin, a cytotoxic 38-membered macrolide, has been disclosed. The key steps involve Sharpless epoxidation, Robinson-Gabriel oxazole synthesis, olefin cross-metathesis, Suzuki coupling, Yamaguchi esterificationn, and Shiina macrolactonization.
URI: http://hdl.handle.net/10397/15916
ISSN: 1861-4728
DOI: 10.1002/asia.201300802
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