1892
DOI: 10.1002/cber.18920250255
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Zur Kenntniss des Amids und Imids der Schwefelsäure

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Cited by 21 publications
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“…[121] In general, the imidazolidinone ring is nearly planar, certainly in the urea region. To determine whether the planar structure future is necessary for the activity, the carbonyl group (sp 2 ) was replaced with the sulfonyl group (sp 3 Diamination of cyclic sulfamide and the mechanism study. [119] Table 6.…”
Section: Catecholsulfatementioning
confidence: 99%
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“…[121] In general, the imidazolidinone ring is nearly planar, certainly in the urea region. To determine whether the planar structure future is necessary for the activity, the carbonyl group (sp 2 ) was replaced with the sulfonyl group (sp 3 Diamination of cyclic sulfamide and the mechanism study. [119] Table 6.…”
Section: Catecholsulfatementioning
confidence: 99%
“…The sulfamide (R 2 NSO 2 NR 2 ) functionality continues to receive widespread attention due to their potential to serve as prospective targets for the development and design of novel small molecule therapeutic agents, agricultural agents, and high‐affinity protein ligands [1,2] . The first synthetic method of the sulfamide formation was reported in 1892 by Traube, who prepared it from sulfuryl chloride and gaseous ammonia [3] …”
Section: Introductionmentioning
confidence: 99%
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“…[11] Moreover, a great variety of binary sulfur nitrogen compounds was explored. Although the synthesis of the first amino sulfur compound SO 2 (NH 2 ) 2 was reported as early as 1892 by Traube, [12] this branch of chemistry did not prosper until the Second World War. The synthesis of the first aliphatic sulfur diimide S(N n Bu) 2 by Goehring and Weis [13] in 1956 gave the so far idle chemical field the necessary impetus for a quick development (cf.…”
Section: General Introductionmentioning
confidence: 99%