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|a Liao, Xuebin
|e verfasserin
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|a Access to the Pyrroloindoline Core via [3 + 2] Annulation as well as the Application in the Synthetic Approach to (±)-Minfiensine
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|c 2016
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|a Text
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|a ohne Hilfsmittel zu benutzen
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|a A [3 + 2] formal cycloaddition reaction using aza-oxyallyl cation as a synthetic synthon was developed to construct the pyrroloindololine core. With this novel method, a variety of C3-substituted indoles were readily converted into the corresponding pyrroloindoline analogues at room temperature in the mixed solvents. To further demonstrate the utility of this method, a synthetic approach to the total synthesis of (±)-minfiensine was developed in quite concise fashion.
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| 700 |
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|a Ji, Wenzhi
|4 oth
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|a Yao, Licheng
|4 oth
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| 773 |
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|i Enthalten in
|t Organic letters
|d Washington, DC [u.a.] : Soc., 1999
|g 18(2016), 3, Seite 628
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|w (DE-600)1458039-1
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|g volume:18
|g year:2016
|g number:3
|g pages:628
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|u http://www.ncbi.nlm.nih.gov/pubmed/26744924
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