145489-91-4Relevant articles and documents
Hypervalent iodine oxidation of α-substituted 2,4-dihydroxyacetophenones: Synthesis of novel o-iodophenoxy ethers via rearrangement of iodonium ylides
Prakash, Om,Sharma, Vijay,Tanwar, Madan P.
, p. 1191 - 1195 (2007/10/03)
α-Substituted 2,4-dihydroxyacetophenones (1a-1i) have been oxidized with phenyliodonium diacetate (PIDA) under three conditions (i) PIDA-KOH-MeOH (basic) at 0°C, (ii) PIDA-MeOH (neutral) at reflux temperature, and (iii) PIDA-AcOH (acidic) at reflux temper
Hypervalent iodine oxidation of some 2,4-dihydroxyacetophenones with iodobenzene diacetate potassium hydroxide in methanol : A novel route to 2-hydroxy-3-iodo-4-phenoxyacetophenones
Prakash, Om,Tanwar, Madan P.,Goyal, Seema,Pahuja, Saroj
, p. 6519 - 6522 (2007/10/02)
Hypervalent iodine oxidation of some 2,4-dihydroxyacetophenones (2a-d) with C6H5I (OAc)2 - KOH/MeOH providing a novel route to 2-hydroxy-3-iodo-4-phenoxyacetophenones (3a-d) via the rearrangement of iodonium ylides is repo