458-07-1Relevant articles and documents
para-Selective Benzylation of Aryl Iodides by the in situ Preparation of ArIF2: a Hypervalent Iodine-Guided Electrophilic Substitution
Chaudhry, Azka,Hyatt, I. F. Dempsey,Im, Haram,Jones, Taro J.,Noorollah, Jennifer,Siddiqi, Fatima,Singh, Nirvanie,Spatola, Nicholas R.
supporting information, (2020/04/16)
Hypervalent iodine-guided electrophilic substitution (HIGES) was described previously for the para-selective benzylation of aryl-λ3-iodane diacetates. One drawback of the method was the synthesis and isolation of hypervalent iodine starting mat
Synthesis of Polysubstituted Iodoarenes Enabled by Iterative Iodine-Directed para and ortho C?H Functionalization
Wu, Yichen,Bouvet, Sébastien,Izquierdo, Susana,Shafir, Alexandr
supporting information, p. 2617 - 2621 (2019/01/04)
Among halogenated aromatics, iodoarenes are unique in their ability to produce the bench-stable halogen(III) form. Earlier, such iodine(III) centers were shown to enable C?H functionalization ortho to iodine via halogen-centered rearrangement. The broader implications of this phenomenon are explored by testing the extent of an unusual iodane-directed para C?H benzylation, as well as by developing an efficient C?H coupling with sulfonyl-substituted allylic silanes. Through the combination of the one-shot nature of the coupling event and the iodine retention, multisubstituted arenes can be prepared by sequentially engaging up to three aromatic C?H sites. This type of iodine-based iterative synthesis will serve as a tool for the formation of value-added aromatic cores.
Use of arene 1,3-substituents to control cyclopropane ring formation during meta photocycloaddition of ethenes to the benzene ring
Amey, David M.,Gilbert, Andrew,Jones, Damian T.
, p. 213 - 218 (2007/10/03)
The 3-trifluoromethyl derivatives of benzyl alcohol, benzyltrimethylsilane and phenoxytrimethylsilane undergo 2,6-photocycloaddition to cyclopentene to give the 1,11-disubstituted-tetracyclo[6.3.0.02,11.0 3,7]-undec-9-enes 7, 10, 11
