Web[Bis (trifluoroacetoxy)iodo]benzene 97% Synonym (s): BTI, Iodobenzene I,I-bis (trifluoroacetate), PIFA Linear Formula: (CF3CO2)2IC6H5 CAS Number: 2712-78-9 Molecular Weight: 430.04 Beilstein: 764767 EC … Web[Bis (trifluoroacetoxy)iodo]benzene is one of numerous organometallic compounds manufactured by American Elements under the trade name AE Organometallics™. Organometallics are useful reagents, catalysts, and precursor materials with applications in thin film deposition, industrial chemistry, pharmaceuticals, LED manufacturing, and others.
An efficient synthesis and biological study of novel indolyl-1,3,4 ...
WebDec 3, 2015 · A practical approach to radical C–H bond functionalization by the photolysis of a hypervalent iodine(III) reagent is presented.The photolysis of [bis(trifluoroacetoxy)iodo]benzene (PIFA) leads to the generation of trifluoroacetoxy radicals, which allows the smooth transformation of various alkylbenzenes to the … WebFeb 24, 2024 · [Bis (trifluoroacetoxy)iodo]benzene Mediated C‐3 Selenylation of Pyrido [1,2‐a]Pyrimidin‐4‐Ones Under Ambient Conditions - Ghosh - 2024 - Advanced Synthesis & Catalysis - Wiley Online Library Full Paper [Bis (trifluoroacetoxy)iodo]benzene Mediated C-3 Selenylation of Pyrido [1,2- a ]Pyrimidin-4-Ones Under Ambient Conditions slay the spire the silent shiv build
[Bis(trifluoroacetoxy)iodo]benzene Mediated C‐3 …
WebAug 1, 2009 · In view of interesting biological activities exhibited by naturally occurring 5- (3′-indolyl) oxazoles and our efforts to search for novel and selective antitumor agents, we report herein [bis (trifluoroacetoxy)iodo]benzene (BTI) mediated synthesis and antitumor activities of analogues 5- (3′-indolyl)-2- (substituted)-1,3,4-oxadiazoles ( 3) under … (Bis(trifluoroacetoxy)iodo)benzene, C 6H 5I(OCOCF 3) 2, is a hypervalent iodine compound used as a reagent in organic chemistry. It can be used to carry out the Hofmann rearrangement under acidic conditions. See more The syntheses of all aryl hypervalent iodine compounds start from iodobenzene. The compound can be prepared by reaction of iodobenzene with a mixture of trifluoroperacetic acid and trifluoroacetic acid in … See more It also brings around the conversion of a hydrazone to a diazo compound, for example in the diazo-thioketone coupling. It also converts thioacetals to their parent carbonyl See more WebMar 1, 2024 · Change of hypervalent iodine-based oxidant to [bis (trifluoroacetoxy) iodo]benzene [PhI (OCOCF3)2] provided 3a in a 58% yield (entry 11). When the oxidant amount was increased from 0.6 to 1.0 mmol or decreased to 0.5 mmol, yield of 3a dropped to 50 and 54%, respectively (entries 12 and 13). slay the spire the board game