62872-49-5Relevant articles and documents
Lewis Base-Promoted Ring-Opening 1,3-Dioxygenation of Unactivated Cyclopropanes Using a Hypervalent Iodine Reagent
Gieuw, Matthew H.,Ke, Zhihai,Yeung, Ying-Yeung
, p. 3782 - 3786 (2018/03/13)
A facile and effective system has been developed for the regio- and chemoselective ring-opening/electrophilic functionalization of cyclopropanes through C?C bond activation by [bis(trifluoroacetoxy)iodo]benzene with the aid of the Lewis basic promoter p-toluenesulfonamide. The p-toluenesulfonamide-promoted system works well for a wide range of cyclopropanes, resulting in the formation of 1,3-diol products in good yields and regioselectivity.
ACTION OF TRIFLUOROACETOXYIODO DERIVATIVES ON PHENYLCYCLOPROPANES
Gazzaeva, R. A.,Shabarov, Yu. A.,Saginova, L. G.
, p. 199 - 200 (2007/10/02)
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REACTION OF SOME PHENYLCYCLOPROPANES WITH IODOSOBENZENE BISTRIFLUOROACETATE
Shabarov, Yu. S.,Pisanova, E. V.,Saginova, L. G.
, p. 1187 - 1188 (2007/10/02)
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