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Hypervalent iodine oxidation of p-alkoxyphenols and related compounds : a general route to p-benzoquinone monoacetals and spiro lactones
Oxydation de dimethoxy-, trimethoxy-, carboxy-2', ethyl, carboxy-2' ethoxy- et hydroxy-2' ethylphenols a l'aide du bis-trifluoroacetoxyiodo benzene
STRUCTURE AND STEREOCHEMISTRY OF NORSECURININE AND DIHYDRONORSECURININE.
Preparation of 5-Aminothiazole-4-carboxylic Acid Derivatives
Cyclization of 2-acylamino-2-thiocarbamoylacetamides (Va, b) with acetic formic anhydride gave good yields of 5-formamidothiazole-4-carboxamides (VIa, b) which were converted toExpand
Cycloaddition of homophthalic anhydride: A new and simple route to linearly condensed phenolic compoumds
Abstract Diels-Alder reaction of homophthalic anhydride ( 1 ) with some dienophiles gave a considerable yield of linearly condensed phenolic compounds, directly.
An efficient conversion of keto groups into dihydroxyacetone groups: Oxidation of ethynylcarbinol intermediates by using hypervalent iodine reagent
Abstract A short and efficient synthesis of dihydroxyacetone groups from keto groups involving the oxidation of ethynylcarbinol intermediates with [bis(trifluoroacetoxy) iodo] benzene (PIFA), isExpand
Stereospecific Epoxidation of cis-2-Butene-1, 4-diones to cis-2, 3-Epoxybutane-1, 4-diones with Oxodiperoxomolybdenum (VI), MoO5·H2O·HMPA
The epoxidation of cis-2-butene-1, 4-diones 4 with (aqua) (hexamethylphosphoramide) oxodiperoxomolybdenum (VI), MoO5·H2O·HMPA, occurred stereospecifically to give the cisepoxides 5, whoseExpand
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