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化學(xué)段落翻譯
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| In an attempt to rationalize all these results, the following mechanism can be proposed (Scheme 3). The catalytic cycle might be initiated by a nucleophilic addition of triphenylphosphine to the electron-deficient allene 2. The enolate 6 then deprotonates the azole 1 generating the nucleophilic species 5 and the vinylphosphonium 4. Consecutively, nucleophilic addition of 5 to vinylphosphonium 4 leads to the ylide 7. Finally, enolate 8 is obtained by prototropy and then undergoes a b-elimination affording the final g-addition allylazole 3 and regenerating the nucleophilic catalyst. |
| 嘗試為這些結(jié)果找合理的理由,推測(cè)的機(jī)理如下(方案3)。催化循環(huán)過程可能是由三苯基磷引發(fā),親核加成到缺電子的丙二烯2上。烯醇6脫去唑1的質(zhì)子生成親核基團(tuán)5 和乙烯基磷4.接著,5親核加成至乙烯基磷生成內(nèi)鎓鹽7.最后,由質(zhì)子轉(zhuǎn)移獲得烯醇化合物8,烯醇化合物8經(jīng)歷β-消除反應(yīng),反應(yīng)提供了最終的g加成的丙烯唑3和再生了親核催化劑。 |

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為了理順?biāo)羞@些結(jié)果,可提出如下方案(方案3)。催化循環(huán)可能由三苯基膦的親核加成到缺電子丙二烯2中所觸發(fā)。然后,烯醇負(fù)離子 6對(duì)唑類1進(jìn)行去除質(zhì)子化,產(chǎn)生了親核物質(zhì)5和乙烯膦4。接著,將5對(duì) 乙烯膦4的親核加成會(huì)產(chǎn)生葉立德7。最后,可通過質(zhì)子移變獲得烯醇負(fù)離子 8。 |
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