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Convenient synthesis of novel macrocyclic urethanes: alkoxycarbonylation of amines and ring-closing metathesis strategy
Alkoxycarbonylation of amines followed by ring-closing metathesis of the resulting dienes with Grubbs catalyst (25–50 mol%) provided convenient access to 14–16 membered macrocyclic urethanes in very good yields. 0 1998 Elsevier Science Ltd. All rights reserved.
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| Pubblicato in: | Tetrahedron Lett |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
1998
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6196740/ https://ncbi.nlm.nih.gov/pubmed/30383041 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0040-4039(98)00153-1 |
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