scholarly journals Effect of 2-[3-(trifluoromethyl)phenyl]-4H-furo[3,2-b]pyrrole-5-carboxhydrazides on photosynthetic processes

2022 ◽  
Vol 7 (1) ◽  
pp. 115-121
Author(s):  
Katarína Kráľová ◽  
Renata Gašparová ◽  
Martin Moncman

A new series of carboxhydrazides 6-8 was synthesized under microwave irradiation by reaction of carboxhydrazide 1 with heterocyclic aldehydes 2-4 in the presence of p-toluenesulfonic acid in ethanol. N-Benzoylcarboxhydrazide 9 was prepared by reaction of 1 with benzoylchlorid 5 in THF at room temperature. The effects of 6-9 on inhibition of photosynthetic electron transport in spinach chloroplasts and chlorophyll content in the antialgal suspensions of Chlorella vulgaris were investigated.

2005 ◽  
Vol 3 (4) ◽  
pp. 622-646 ◽  
Author(s):  
Renata Ga<parová ◽  
Daniel Zbojek ◽  
Margita Lácová ◽  
Katarína Král'ová ◽  
Anton Gatial ◽  
...  

AbstractThe reactions of substituted furo[3,2-b]pyrrole-5-carboxhydrazides 1 with 5-arylfuran-2-carboxaldehydes 2, 4,5-disubstituted furan-2-carboxaldehydes 3 and thiophene-2-carboxaldehyde 4 has been studied. The advantage of microwave irradiation on some of these reactions was reflected in the reduced reaction time and increased yields. Reactions of 1 with 4-substituted 1,3-oxazol-5(4H)-ones 11 led to diacylhydrazines 13 or to imidazole derivatives 14 depending on the temperature. 1,2,4-Triazole-3-thione 17 was synthesized by two-step reaction of 1 with phenylisothiocyanate and subsequent base-catalyzed cyclization of thiosemicarbazide 16. The effects of hydrazones 5–10 on inhibition of photosynthetic electron transport in spinach chloroplasts and chlorophyll content in the antialgal suspensions of Chlorella vulgaris were investigated.


1987 ◽  
Vol 891 (1) ◽  
pp. 75-84 ◽  
Author(s):  
Magdolna Droppa ◽  
Jiři Masojidek ◽  
Zsuzsanna Rózsa ◽  
Adam Wolak ◽  
LászlóI. Horváth ◽  
...  

1981 ◽  
Vol 36 (9-10) ◽  
pp. 848-852 ◽  
Author(s):  
W. Draber ◽  
H. J. Knops ◽  
A. Trebst

Abstract Several substituted diphenylethers were found to be effective inhibitors of photosynthetic electron flow in isolated thylakoid membranes from spinach chloroplasts. T heir site of inhibition was localized with artificial acceptor and donor systems. The phenylether of an alkyl substituted nitrophenol is prim arely inhibiting electron flow after plastoquinone function whereas a dinitro-phenylether of a phenyl substituted nitrophenol is inhibiting before plastoquinone function. Therefore certain diphenylethers interfere with plastoquinone function at the oxidation or reduction site, depending on the substitution.


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