Alcohols can be converted in high yields to the corresponding alkyl halides in a one-pot procedure via the corresponding O-alkylisourea; very short reaction times are possible when microwave irradiation is used
An easily accessible ionic liquid, 1-methyl-3-pentylimidazolium fluoroborate, [pmIm]BF<SUB>4</SUB>, ...
Stable allylboronates with a stereogenic centre α to the boronic ester moiety represent versatile re...
The conversion of alcohols into alkyl halides is one of the most important reactions in organic chem...
Alcohols can be converted in high yields to the corresponding alkyl halides in a one-pot procedure v...
The formation of carboxylic esters via reaction of carboxylic acids with O-alkylisoureas proceeds in...
The formation of carboxylic esters via reaction of carboxylic acids with O-alkylisoureas proceeds in...
A simple Lewis acid-mediated route for the synthesis of alkenyl halides are described under microwav...
A simple, mild and one-pot straightforward microwave-assisted route for the synthesis of alkenyl ha...
The present work reports a study on the isomerization reactions of several alkyl epoxides to the cor...
A simple and effective procedure for conversion of primary, secondary, allylic and benzylic alcohols...
Fused heterocyclic compounds with alkyne substituent, have been achieved using a domino microwave-as...
Combination of iodine and triphenylphosphine in the presence of a slight stoichiometric excess of 2,...
Abstract: Non-conventional techniques, such as microwave (MW) and power ultrasound (US) as well as c...
A combination of benzyltriethylammonium borohydride and chlorotrimethylsilane (1:1) in dichlorometha...
A variety of symmetrical N,N'-disubstituted thioureas have been prepared by a simple reaction of ami...
An easily accessible ionic liquid, 1-methyl-3-pentylimidazolium fluoroborate, [pmIm]BF<SUB>4</SUB>, ...
Stable allylboronates with a stereogenic centre α to the boronic ester moiety represent versatile re...
The conversion of alcohols into alkyl halides is one of the most important reactions in organic chem...
Alcohols can be converted in high yields to the corresponding alkyl halides in a one-pot procedure v...
The formation of carboxylic esters via reaction of carboxylic acids with O-alkylisoureas proceeds in...
The formation of carboxylic esters via reaction of carboxylic acids with O-alkylisoureas proceeds in...
A simple Lewis acid-mediated route for the synthesis of alkenyl halides are described under microwav...
A simple, mild and one-pot straightforward microwave-assisted route for the synthesis of alkenyl ha...
The present work reports a study on the isomerization reactions of several alkyl epoxides to the cor...
A simple and effective procedure for conversion of primary, secondary, allylic and benzylic alcohols...
Fused heterocyclic compounds with alkyne substituent, have been achieved using a domino microwave-as...
Combination of iodine and triphenylphosphine in the presence of a slight stoichiometric excess of 2,...
Abstract: Non-conventional techniques, such as microwave (MW) and power ultrasound (US) as well as c...
A combination of benzyltriethylammonium borohydride and chlorotrimethylsilane (1:1) in dichlorometha...
A variety of symmetrical N,N'-disubstituted thioureas have been prepared by a simple reaction of ami...
An easily accessible ionic liquid, 1-methyl-3-pentylimidazolium fluoroborate, [pmIm]BF<SUB>4</SUB>, ...
Stable allylboronates with a stereogenic centre α to the boronic ester moiety represent versatile re...
The conversion of alcohols into alkyl halides is one of the most important reactions in organic chem...
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