An efficient one-pot method for the synthesis of cyanamides from dithiocarbamate salts via a double desulfurization strategy using molecular iodine is disclosed. Dithiocarbamates, by the action of iodine yield isothiocyanates in situ, which on treatment with aqueous NH3 give thioureas. The thioureas so generated undergo further oxidative desulfurization with I2 giving corresponding cyanamides in good yields. Environmental benignity, cost effectiveness and high yields are the important attributes of this one pot procedure
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
A simple and cost-effective one-pot parallel synthesis approach to sulfides, sulfoxides, and sulfone...
A novel methodology for the synthesis of S- and N-functionalized dithiocarbamates starting from cycl...
An efficient one-pot method for the synthesis of cyanamides from dithiocarbamate salts via a double ...
In a one-pot strategy we have achieved an efficient method for the synthesis of organic cyanamides s...
An environmentally benign reaction is devised for the synthesis of cyanamides from dithiocarbamate s...
We report here an improved procedure for the synthesis of isothiocyanates from the corresponding dit...
n a one-pot procedure, bromineless brominating reagent 1,1′-(ethane-1,2-diyl)dipyridinium bistribrom...
We have developed a general economical and environmentally benign method for the preparation of isot...
In the present study, the utility of the hypervalent iodine(III) reagent, diacetoxyiodobenzene is ex...
The desulfurization ability of diacetoxyiodobenzene (DIB) has been explored in the preparation of is...
A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothio...
Synthetic methods providing access to sulfonylureas are immensely valuable considering the wide usag...
A one-pot preparation of pyridyl isothiocyanates (ITCs) from their corresponding amines has been dev...
A one-pot synthesis of 3-amino-1,3,4-oxadiazoles has been achieved from the corresponding dithiocarb...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
A simple and cost-effective one-pot parallel synthesis approach to sulfides, sulfoxides, and sulfone...
A novel methodology for the synthesis of S- and N-functionalized dithiocarbamates starting from cycl...
An efficient one-pot method for the synthesis of cyanamides from dithiocarbamate salts via a double ...
In a one-pot strategy we have achieved an efficient method for the synthesis of organic cyanamides s...
An environmentally benign reaction is devised for the synthesis of cyanamides from dithiocarbamate s...
We report here an improved procedure for the synthesis of isothiocyanates from the corresponding dit...
n a one-pot procedure, bromineless brominating reagent 1,1′-(ethane-1,2-diyl)dipyridinium bistribrom...
We have developed a general economical and environmentally benign method for the preparation of isot...
In the present study, the utility of the hypervalent iodine(III) reagent, diacetoxyiodobenzene is ex...
The desulfurization ability of diacetoxyiodobenzene (DIB) has been explored in the preparation of is...
A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothio...
Synthetic methods providing access to sulfonylureas are immensely valuable considering the wide usag...
A one-pot preparation of pyridyl isothiocyanates (ITCs) from their corresponding amines has been dev...
A one-pot synthesis of 3-amino-1,3,4-oxadiazoles has been achieved from the corresponding dithiocarb...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
A simple and cost-effective one-pot parallel synthesis approach to sulfides, sulfoxides, and sulfone...
A novel methodology for the synthesis of S- and N-functionalized dithiocarbamates starting from cycl...