80550-04-5Relevant academic research and scientific papers
Synthesis, reactivity, and antimicrobial properties of boron-containing 4-ethyl-3-thiosemicarbazide derivatives
Scott, Ryan S.,Veinot, Alex J.,Stack, Darcie L.,Gormley, Patrick T.,Khuong, B. Ninh,Vogels, Christopher M.,Masuda, Jason D.,Baerlocher, Felix J.,Maccormack, Tyson J.,Westcott, Stephen A.
, p. 906 - 911 (2018)
The addition of 4-ethyl-3-thiosemicarbazide to benzaldehyde and boronic acid containing derivatives afforded the corresponding thiosemicarbazones (1-3) or benzodiazaborines (4-6) depending on the position of the boronic acid within the ring. All compounds
The influence of benzaldehyde-N-alkyl-thiosemicarbazones on the synthesis of gold(I) ionic complexes: Spectroscopy, ESI-mass, structures and variable H-bonded polymeric networks
Lobana, Tarlok S.,Sharma, Rekha,Indoria, Shikha,Butcher, Ray J.
supporting information, p. 89 - 97 (2015/03/30)
The effect of the substituents at the N1/C2 atoms of the thiosemicarbazones R1R2C2 = N3-N2H-C1(=S)-N1HR3 on the type of gold(I) complexes is inve
Unexpected ring enlargement of 2-hydrazono-2,3-dihydro-1,3-thiazoles to 1,3,4-thiadiazines
Pfeiffer, Wolf-Diethard,Ahlers, Klaus-Dieter,Saghyan, Ashot S.,Villinger, Alexander,Langer, Peter
, p. 76 - 87 (2014/02/14)
The cyclization of thiosemicarbazide with α-bromoacetophenone can result in the formation of isomeric 1,3,4-thiadiazines and two different thiazoles. We studied the use of 4-methyl- and 4-ethylthiosemicarbazide as dinucleophilic building blocks. In this c
