Add to ORKGBenzyltriethylammonium tetrathiomolybdate, $[BnEt_3N]_2MoS_4$, has been used successfully to effect ring opening of aziridines in a regiospecific and stereospecific manner under mild reaction conditions without the use of Lewis acid catalyst. Utility of this reagent in tandem and multistep processes in a one-pot operation for the synthesis of various novel sulfur heterocycles in very good yield is also reported
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
A comprehensive study of a general and effective one-step procedure for the synthesis of $\beta$-sul...
A comprehensive study of a general and effective one-step procedure for the synthesis of $\beta$-sul...
Benzyltriethylammonium tetrathiomolybdate, $[BnEt_3N]_2MoS_4$, has been used successfully to effect ...
A detailed study of tetrathiomolybdate mediated tandem regio- and stereoselective ring opening of az...
A detailed study of tetrathiomolybdate mediated tandem regio- and stereoselective ring opening of az...
Direct synthesis of unsymmetrical beta-sulfonamido disulfides by ring-opening of aziridines by using...
Direct synthesis of unsymmetrical beta-sulfonamido disulfides by ring-opening of aziridines by using...
The thesis entitled “Chemistry of Tetrathiomolybdate and Tetraselenotungstate: Studies on Aziridine ...
The utility of tetrathiomolybdate in a variety of organic transformations is presented in this accou...
Here we present a new synthetic process of aziridine and azetidine NRORs with metal halides and othe...
Aziridine and azetidine moieties are important small ring N-heterocycles in organic synthesis due to...
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
Here we present a new synthetic process of aziridine and azetidine nucleophilic ring opening reactio...
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
A comprehensive study of a general and effective one-step procedure for the synthesis of $\beta$-sul...
A comprehensive study of a general and effective one-step procedure for the synthesis of $\beta$-sul...
Benzyltriethylammonium tetrathiomolybdate, $[BnEt_3N]_2MoS_4$, has been used successfully to effect ...
A detailed study of tetrathiomolybdate mediated tandem regio- and stereoselective ring opening of az...
A detailed study of tetrathiomolybdate mediated tandem regio- and stereoselective ring opening of az...
Direct synthesis of unsymmetrical beta-sulfonamido disulfides by ring-opening of aziridines by using...
Direct synthesis of unsymmetrical beta-sulfonamido disulfides by ring-opening of aziridines by using...
The thesis entitled “Chemistry of Tetrathiomolybdate and Tetraselenotungstate: Studies on Aziridine ...
The utility of tetrathiomolybdate in a variety of organic transformations is presented in this accou...
Here we present a new synthetic process of aziridine and azetidine NRORs with metal halides and othe...
Aziridine and azetidine moieties are important small ring N-heterocycles in organic synthesis due to...
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
Here we present a new synthetic process of aziridine and azetidine nucleophilic ring opening reactio...
Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as t...
A comprehensive study of a general and effective one-step procedure for the synthesis of $\beta$-sul...
A comprehensive study of a general and effective one-step procedure for the synthesis of $\beta$-sul...