Convenient one-pot access to 2H-3-nitro-thiochromenes from 2-bromobenzaldehydes, sodium sulfide and β-nitrostyrenes

Convenient one-pot access to 2H-3-nitro-thiochromenes from 2-bromobenzaldehydes, sodium sulfide and β-nitrostyrenes
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方便地从 2-溴苯甲醛、硫化钠和 β-硝基苯乙烯中一锅法制备 2H-3-硝基硫色烯

DOI:
10.1039/c9ob01060b
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发表时间:
2019
期刊:
Org. Biomol. Chem.
影响因子:
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通讯作者:
Dinh Hung Mac
Dinh Hung Mac
中科院分区:
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文献类型:
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作者:
Thi Thu Huong Le;Chitose Youhei;Quy Hien Le;Thanh Binh Nguyen;Dinh Hung Mac

文献摘要

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建立了用级联反应高效合成2h -3-亚硝基铬的方法。以市售的邻溴苯甲醛和β-亚硝基苯乙烯为原料,以非水合硫化钠为廉价硫源,在不添加任何过渡金属催化剂或添加剂的情况下,合成了各种具有高官能团耐受性的取代硫代铬。
An efficient synthesis of 2H-3-nitrothiochromenes via a cascade reaction was established. Starting from commercially available o-bromobenzaldehydes and β-nitrostyrenes with sodium sulfide nonahydrate as an inexpensive sulfur source, various substituted thiochromenes were synthesized with high functional group tolerance without any added transition metal catalyst or additive.