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Article . 2015 . Peer-reviewed
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A concise formal total synthesis of lactimidomycin
Authors: Wei Li; Gunda I. Georg;
pmid: 25900419
A concise formal total synthesis of lactimidomycin
Abstract
An ene–yne coupling/alkyne reduction tandem ring-closing reaction was employed for the formal total synthesis of the anti-tumor natural product lactimidomycin.
Related Organizations
- University of Minnesota Morris United States
Keywords
Biological Products, Molecular Conformation, Macrolides, Piperidones
Biological Products, Molecular Conformation, Macrolides, Piperidones
14 Research products, page 1 of 2
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citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
popularity
Popularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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