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Fluoroalcohol-mediated reductive iodonio-Claisen rearrangement: Synthesis of complex ortho-substituted-allyl iodoarenes 被引量:4
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作者 hem raj khatri hai nguyen james k. dunaway jianglong zhu 《Frontiers of Chemical Science and Engineering》 SCIE EI CAS CSCD 2015年第3期359-368,共10页
Reductive iodonio-Claisen rearrangement (RICR) involving 23-iodanes and allyl or substituted-allyl silanes in fluoroalcohols, such as 1,1,1,3,3,3-hexafluoroi- sopropanol (HFIP) and 2,2,2-trifluoroethanol (TFE), ... Reductive iodonio-Claisen rearrangement (RICR) involving 23-iodanes and allyl or substituted-allyl silanes in fluoroalcohols, such as 1,1,1,3,3,3-hexafluoroi- sopropanol (HFIP) and 2,2,2-trifluoroethanol (TFE), was studied for the synthesis of complex ortho-allyl or substituted-allyl iodoarenes. In comparison to the pre- viously reported condition involving boron trifluoride diethyl etherate, the RICR mediated by fluoroalcohols was found to proceed more effectively. The resulting complex ortho-allyl iodoarenes are useful synthetic intermediates and can be readily converted to various heterocyclic compounds. 展开更多
关键词 hypervalent iodine ALLYLATION FLUOROALCOHOL Claisen rearrangement HETEROCYCLES
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