1999
DOI: 10.1016/s0040-4039(98)02361-2
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Aryl chlorothionoformate: A new versatile reagent for the preparation of nitriles and isonitriles under mild conditions

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Cited by 34 publications
(15 citation statements)
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“…Chlorothionofomate esters are useful as derivatizing agents [1] and common organic building blocks in the synthesis of commercial thiocarbonate esters, nitriles, and isonitriles [2,3]. High fungicidal activity was demonstrated [4] for the p -substituted aryl thiocarbamate analogs which are also cytotoxic [5].…”
Section: Introductionmentioning
confidence: 99%
“…Chlorothionofomate esters are useful as derivatizing agents [1] and common organic building blocks in the synthesis of commercial thiocarbonate esters, nitriles, and isonitriles [2,3]. High fungicidal activity was demonstrated [4] for the p -substituted aryl thiocarbamate analogs which are also cytotoxic [5].…”
Section: Introductionmentioning
confidence: 99%
“…have been described in the literature. Some of them require basic reactives and lead to the attainment of carbonitriles [26] and carbodiimides [27][28][29][30][31]. In some cases, the attack of a basic reactive as sodium methoxide to the thioamide carbon atom has been proposed [32].…”
mentioning
confidence: 99%
“…Up to now manifold syntheses have been established to access nitriles. Among those protocols the dehydration of amides is an attractive approach and diverse reagent to perform this reaction have been introduced [2][3][4][5][6][7][8][9][10][11][12][13][14][15]. However, the application of stoichiometric amounts of highly acidic and basic compounds disfavors the dehydration of sensitive substrate and reduces the generality of the methods.…”
Section: Introductionmentioning
confidence: 99%