scholarly journals Sodium azide mutagenesis in diploid and hexaploid oats and comparison with ethyl methanesulfonate treatments

1985 ◽  
Vol 25 (1) ◽  
pp. 7-16 ◽  
Author(s):  
H.W. Rines
1984 ◽  
Vol 6 (3) ◽  
pp. 311-320 ◽  
Author(s):  
James M. Lavelle ◽  
Charlotte M. Witmer

1987 ◽  
Vol 67 (3) ◽  
pp. 909-917 ◽  
Author(s):  
T. A. CAMPBELL

Presoaked (24 h at 20 °C) seeds of Cuphea tolucana Peyr. and C. wrightii A. Gray were treated with mutagens at 20 °C in two experiments. Experiment 1 treatments were: distilled water (DW), 0.05 M PO4 buffer (pH 7), 0.01 M ethyl methanesulfonate (EMS) (each applied for 8 h), 0.02 M EMS (applied for 4 h), 0.04 EMS M, 0.08 M EMS, or 0.16 M EMS (each applied for 2 h). Experiment 2 treatments were: DW, 0.1 M PO4 buffer (pH 3), 0.0005 M sodium azide (SA), 0.001 M SA, or 0.002 M SA (each applied for 2 h). None of the treatments had significant effects on emergence and height of M1 plants nor were any macro-mutations noted in the M2 generations. In a third experiment, DW, 0.04 M EMS, or 0.001 M SA were applied for 2 h at 30 °C to presoaked (48 or 72 h at 30 °C) seeds of C. tolucana and C. wrightii. Compared to EMS, SA had deleterious effects on height in the M1, emergence was better for C. tolucana than for C. wrightii, and C. wrightii plants grew taller after a 72-h pre-soak than after a 48-h presoak. M2 progenies were evaluated in the field. None of the presoak-treatment combinations increased variation significantly in several quantitative characters, no macro-mutations were detected in C. wrightii, but a fertile, small-leaved, decumbent mutant with very short internodes was noted in C. tolucana. Mutation rates were greatest for the 72 h presoak-EMS combination.Key words: Cuphea tolucana, Cuphea wrightii, ethyl methanesulfonate, sodium azide, medium-chain triglycerides, lauric acid


2020 ◽  
Vol 24 (4) ◽  
pp. 439-464 ◽  
Author(s):  
Rizk E. Khidre ◽  
Tahah A. Ameen ◽  
Mounir A. I. Salem

This review summarizes the synthesis, reactions, and biological activities of tetrazolo[1,5-a]quinoline derivatives. These derivatives were synthesized by several methods such as i) from the reaction of 2-chloroquinoline with sodium azide ii) from diazotization 2-hydrazinylquinoline derivatives, and iii) from intramolecular cyclocondensation of 2-azidoarylidenes. Also, the chemical reactions and pharmacological activities of some tetrazoloquinolines such as tetrazolo[1,5-a]quinoline-4-carbaldehyde, 5-chlorotetrazolo[ 1,5-a]quinoline, 4-(chloromethyl)tetrazolo[1,5-a]quinoline, tetrazolo[1,5- a]quinoline-4-carboxylic acid, and 5-azidotetrazolo[1,5-a]quinoline were discussed.


1980 ◽  
Vol 45 (12) ◽  
pp. 3378-3390 ◽  
Author(s):  
Jiří Jarý ◽  
Milena Masojídková ◽  
Ivan Kozák ◽  
Miroslav Marek ◽  
Jan Staněk

The title amino derivatives VI and XIV were prepared by nucleophilic substitution of p-toluenesulfonyl derivatives II and XVII with sodium azide or hydrazine and subsequent reduction. Nucleophilic substitution of compounds II and XVII with sodium benzoate was also investigated. The 1H NMR spectra of the substances prepared are discussed.


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