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Reversible Dimerization of (+)-Myrmicarin 215B
[Image: see text] Brønsted acid-promoted reversible dimerization of myrmicarin 215B leads to formation of a new heptacyclic product, isomyrmicarin 430B, that possesses a C1,C2-trans, C2,C3-trans substituted cyclopentane ring. Mechanistic studies illustrate that isomyrmicarin 430B arises by isomeriza...
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| Main Authors: | , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2009
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2752850/ https://ncbi.nlm.nih.gov/pubmed/19586059 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol9008552 |
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