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通过2,4-二碘-1-丁烯与芳基硼酸和格氏试剂的铃木-宫浦和熊田交叉偶联策略简便合成多取代1,3-丁二烯。

Facile synthesis of multisubstituted buta-1,3-dienes via Suzuki-Miyaura and Kumada cross-coupling strategy of 2,4-diiodo-buta-1-enes with arylboronic acids and Grignard reagents.

作者信息

Shao Li-Xiong, Shi Min

机构信息

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Fenglin Lu, Shanghai, China.

出版信息

Org Biomol Chem. 2005 May 21;3(10):1828-31. doi: 10.1039/b504071j. Epub 2005 Apr 12.

Abstract

One-pot Suzuki-Miyaura-type and Kumada-type cross-coupling reactions of 2,4-diiodo-buta-1-enes with arylboronic acids and alkyl/aryl magnesium bromides were carried out in the presence of accessibly simple catalysts under mild conditions. As a result, some 1,1,2-trisubstituted buta-1,3-dienes were obtained including the Tamoxifen-type, which have potential adjuvant therapy in women who have suffered from breast cancer and cyclooxygenase-2-type (COX-2-type) inhibitors, some of which have been proved to elicit efficient anti-inflammatory analgesic activities and less adverse gastrointestinal side effects and to be very useful in the prophylactic treatment of a wide variety of cancers and neurodegenerative disorders.

摘要

在温和条件下,以易于制备的简单催化剂为存在,使2,4-二碘-1-丁烯与芳基硼酸以及烷基/芳基溴化镁进行一锅法铃木-宫浦型和熊田型交叉偶联反应。结果得到了一些1,1,2-三取代-1,3-丁二烯,包括他莫昔芬型,其在患有乳腺癌的女性中具有潜在的辅助治疗作用,以及环氧化酶-2型(COX-2型)抑制剂,其中一些已被证明能产生有效的抗炎镇痛活性且胃肠道副作用较小,在多种癌症和神经退行性疾病的预防性治疗中非常有用。

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