Ferdinand,G. et al., Justus Liebigs Annalen der Chemie, 1976, p. 1713 - 1726
作者:Ferdinand,G. et al.
DOI:——
日期:——
Intramolecular acid-catalyzed reactions of o-carbomethoxy-?-diazoacetophenones
作者:S. V. Chapyshev、L. I. Kurkovskii、V. G. Kartsev
DOI:10.1007/bf00962316
日期:1987.4
Oxidative rearrangements of arylalkanones with 1H-1-hydroxy-5-methyl-1,2,3-benziodoxathiole 3,3-dioxide, a ‘green’ analog of Koser’s reagent
作者:Michael W. Justik
DOI:10.1016/j.tetlet.2007.02.129
日期:2007.4
Previous methods for the conversion of arylalkanones to alkyl 2-arylesters by oxidative rearrangement utilized reagents which either produced toxic metal salts or halogenated organics as by-products. In this report, 1H-1-hydroxy-5-methyl-1,2,3-benziodoxathiole 3,3-dioxide (HMBI) is used to effect this useful transformation, where the reduced iodine reagent is water-soluble and readily recycled. (c) 2007 Elsevier Ltd. All rights reserved.
Prakash; Goyal; Moriatry, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1990, vol. 29, # 4, p. 304 - 309
作者:Prakash、Goyal、Moriatry、Khosrowshahi
DOI:——
日期:——
Hypervalent iodine oxidation of silyl enol ethers under Lewis-acid conditions in methanol. A general route to .alpha.-methoxy ketones
作者:Robert M. Moriarty、Om Prakash、Michael P. Duncan、Radhe K. Vaid、Hikmat A. Musallam