Histochemical localization of urushiols in stems and leaflets of Schinopsis lorentzii and S. marginata using diazonium salts

Flora ◽  
2017 ◽  
Vol 236-237 ◽  
pp. 25-32
Author(s):  
Diego A. Sampietro ◽  
María I. Mercado ◽  
María E. Aristimuño Ficoseco ◽  
Graciela Ponessa ◽  
Marta A. Vattuone ◽  
...  
2019 ◽  
Author(s):  
Clara M. Agapie ◽  
Melissa Sampson ◽  
William Gee

The work describes a new chemical means of visualising latent fingerprints (fingermarks) using tropolone. Tropolone reacts with amino acids within the fingermark residue to form adducts that absorb UV radiation. These adducts provide useful contrast on highly-fluorescent prous surfaces will illuminated with UV radiation. The conjugated seven-membered ring of the tropolone adduct can be reacted further diazonium salts, which is demonstrated here with formation of two dyes. The methodology is extremely rapid, occurring in minutes with mild heating, and can be applied before ninhydrin in a chemical detection sequence. <br>


1949 ◽  
Vol 68 (5) ◽  
pp. 426-429 ◽  
Author(s):  
J. de Jonge ◽  
R. Dijkstra
Keyword(s):  

2020 ◽  
Vol 21 (12) ◽  
pp. 2827-2835
Author(s):  
P. R. Hande ◽  
P. P. Badve ◽  
R. G. Dugane ◽  
S. S. Bhagwat ◽  
P. M. Bhate

Oral Diseases ◽  
2021 ◽  
Author(s):  
Yan Wu ◽  
Caixia Zhou ◽  
Xueying Tong ◽  
Shue Li ◽  
Jiarong Liu

1999 ◽  
Vol 23 (11) ◽  
pp. 648-649
Author(s):  
Abdul Aziz Al-Naggar ◽  
Mervat Mohammed Abdel-Khalik ◽  
Mohammed Hilmy Elnagdi

Benzotriazolylacetone is coupled with aromatic diazonium salts to yield arylhydrazones, which can be condensed with ethyl cyanoacetate yielding pyridazinones whose reactivity towards activated double bond systems is investigated.


2021 ◽  
pp. 100077
Author(s):  
Audrey McAlinden ◽  
David M. Hudson ◽  
Aysel A. Fernandes ◽  
Soumya Ravindran ◽  
Russell J. Fernandes

2020 ◽  
Vol 18 (9) ◽  
pp. 1812-1819 ◽  
Author(s):  
Elene Tatunashvili ◽  
Bun Chan ◽  
Philippe E. Nashar ◽  
Christopher S. P. McErlean

Hantzsch esters and oxygen convert diazonium salts into aryl radicals, enabling rapid radical reactions to be performed in open flasks at room temperature.


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