1992
DOI: 10.1080/01961779208048943
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Thioformyl Compounds. Synthesis, Structure and Properties

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Cited by 22 publications
(11 citation statements)
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“…[54] Thioaldehydes can react with amines and thiols to form imines, [55] disulfides, [56] and oximes (Figure 5a). [54] Thioaldehydes can react with amines and thiols to form imines, [55] disulfides, [56] and oximes (Figure 5a).…”
Section: Methodsmentioning
confidence: 99%
“…[54] Thioaldehydes can react with amines and thiols to form imines, [55] disulfides, [56] and oximes (Figure 5a). [54] Thioaldehydes can react with amines and thiols to form imines, [55] disulfides, [56] and oximes (Figure 5a).…”
Section: Methodsmentioning
confidence: 99%
“…Thioaldehydes are prone to intra-and intermolecular transformations [12]. The mechanism of these reactions is poorly understood, mainly due to difficulties in experimental kinetic studies.…”
Section: Methodsmentioning
confidence: 99%
“…They were long thought to be extremely unstable and therefore remained poorly understood. However, interest in their synthetic and applied chemistry has greatly increased due to studies carried out in different countries [12,15,16].…”
Section: Methodsmentioning
confidence: 99%
“…The ability of thioaldehydes to form trimers is well known. It was also noted that hydroxy-containing solvents favor the trimerization process [2]. We performed quantum-chemical analysis of possible structural transformations of thioaldehyde II and revealed its ability to undergo trimerization in polar medium [3].…”
mentioning
confidence: 99%