1980
DOI: 10.1055/s-1980-28939
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A New Synthesis of Diacylamines

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Cited by 41 publications
(9 citation statements)
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“…To make N‐Boc derivatives available by substitution under salt‐free conditions, we probed the new prenucleophile HN(Boc)(CHO), which was expected to be more acidic than HNBoc 2 . This readily available compound14 indeed gave excellent results with respect to yield as well as regio‐and enantioselectivity (Table 2, entries 10–13).…”
Section: Methodsmentioning
confidence: 85%
“…To make N‐Boc derivatives available by substitution under salt‐free conditions, we probed the new prenucleophile HN(Boc)(CHO), which was expected to be more acidic than HNBoc 2 . This readily available compound14 indeed gave excellent results with respect to yield as well as regio‐and enantioselectivity (Table 2, entries 10–13).…”
Section: Methodsmentioning
confidence: 85%
“…Yield: 44.7 mg (43%); yellow solid; mp 221-223 °C (Lit. 28 3250, 1706, 1582, 1505, 1476, 1228, 1178, 1118, 1073, 1026, 710 cm -1 .…”
Section: N-acetyl-4-nitrobenzamide (2f) 29mentioning
confidence: 99%
“…As shown, excellent yields were obtained in the reactions of aliphatic nitriles (entries 1-9). In the case of aryl nitriles, the corresponding amides were also produced as side products, therefore the yields decreased in these cases (entries [10][11][12][13][14][15][16]. We decided to conduct the same reaction with other typical Lewis acids such as AlCl 3 , FeCl 3 , ZnCl 2 , NaHSO 4 , etc.…”
Section: Methodsmentioning
confidence: 99%