2018
DOI: 10.1016/j.tetlet.2018.08.058
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Synthesis of the trisoxazole macrolactone of mycalolides via template-directed E-selective ring-closing metathesis

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Cited by 3 publications
(2 citation statements)
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“…It is also worth noting that in the field of natural products synthesis, RCM has been used to realize the synthesis of complex molecules such as the synthesis of the 15‐membered heteroatom macrocyclic compound HCV Protease Inhibitor BILN 2061, the formation of analogues of the peptide hormone Oxytocin, macrolide analogues of the immunosuppressant Sanglifehrin, the synthesis of the trisoxazole macrolactone of mycalolides A and B, and more . While these structures were not intended for further polymerization, these synthetic efforts highlight the full potential of RCM for a further broadening of functional macrocycles that can be envisioned in the future.…”
Section: Macrocycle Synthesismentioning
confidence: 99%
“…It is also worth noting that in the field of natural products synthesis, RCM has been used to realize the synthesis of complex molecules such as the synthesis of the 15‐membered heteroatom macrocyclic compound HCV Protease Inhibitor BILN 2061, the formation of analogues of the peptide hormone Oxytocin, macrolide analogues of the immunosuppressant Sanglifehrin, the synthesis of the trisoxazole macrolactone of mycalolides A and B, and more . While these structures were not intended for further polymerization, these synthetic efforts highlight the full potential of RCM for a further broadening of functional macrocycles that can be envisioned in the future.…”
Section: Macrocycle Synthesismentioning
confidence: 99%
“…Dentre as diversas classes existentes 37 , a reação de metátese está entre as mais comuns e eficientes. A reação de metátese tem sido aplicada na síntese de diferentes produtos naturais [38][39][40]…”
Section: Reação De Metáteseunclassified