首页> 外文期刊>The Journal of Organic Chemistry >Atom-Transfer Cyclization with CuSO4/KBH4: A Formal “Activators Generated by Electron Transfer” Process Also Applicable to Atom-Transfer Polymerization
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Atom-Transfer Cyclization with CuSO4/KBH4: A Formal “Activators Generated by Electron Transfer” Process Also Applicable to Atom-Transfer Polymerization

机译:CuSO4 / KBH4的原子转移环化:正式的“由电子转移产生的活化剂”工艺也适用于原子转移聚合

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摘要

The 4-exo and 5-exo-trig atom-transfer cyclizations of 1, 8a–e, 9, 12, and 13 can be mediated with as little as 0.05 mol % of Cu(TPMA)SO4·5H2O in the presence of 2.5 mol % of borohydride salts in 10 min at room temperature in air. This formal “activators generated by electron transfer” (AGET) procedure utilizes a cheap and oxidatively stable copper source (CuSO4·5H2O) and can be carried out in environmentally benign solvents (EtOH). It is possible to alter the product distribution in the 5-endo radical–polar crossover reactions of 10a,b and 11 by tailoring the amount of borohydride. Cyclization onto alkynes 14 and 15 is also possible in only 20 min. Controlled radical polymerization of styrene, with increased rates over conventional atom-transfer radical polymerization (ATRP), can be carried out in a controlled fashion (Mn, PDI) using either CuBr or CuSO4·5H2O and Bu4NBH4.
机译:在存在2.5的条件下,仅需0.05 mol%的Cu(TPMA)SO4·5H2O即可介导1、8a-e,9、12和13的4-exo和5-exo-trig原子转移环化反应室温下在空气中10分钟内的mol%硼氢化盐。这种正式的“通过电子转移产生的活化剂”(AGET)程序利用廉价且氧化稳定的铜源(CuSO4·5H2O),可以在环境友好的溶剂(EtOH)中进行。通过调整硼氢化物的量,可以改变10a,b和11的5内基自由基-极性交叉反应中的产物分布。仅在20分钟内也可以环化到炔烃14和15上。可以使用CuBr或CuSO4·5H2O和Bu4NBH4以受控方式(Mn,PDI)进行苯乙烯的受控自由基聚合,其速率比常规原子转移自由基聚合(ATRP)高。

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