ChemInform Abstract: N-ARYL ALKYL CARBAMATE DERIVATIVES OF TANTALUM(V)

1978 ◽  
Vol 9 (12) ◽  
Author(s):  
R. BOHRA ◽  
A. K. RAI ◽  
R. C. MEHROTRA
1977 ◽  
Vol 25 ◽  
pp. L147-L148 ◽  
Author(s):  
R. Bohra ◽  
A.K. Rai ◽  
R.C. Mehrotra

Weed Science ◽  
1975 ◽  
Vol 23 (5) ◽  
pp. 425-427 ◽  
Author(s):  
R. S. Hammerschlag ◽  
J. L. Hilton ◽  
P. G. Bartels ◽  
D. E. Moreland

Inhibition of seedling growth and four assays for inhibition of photosynthesis were used to compare karbutilate [tert-butylcarbamic acid ester with 3-(m-hydroxyphenyl)-1,1-dimethylurea] with derivatives of karbutilate in which either the urea or carbamate side chain was missing. Karbutilate was a more potent, more presistent, and more specific inhibitor of photosynthesis than the phenylurea derivative fenuron (1,1-dimethyl-3-phenylurea) that would be formed by removal of the carbamate side chain. However, karbutilate did not exert the growth-inhibiting action observed for the alkyl carbamate derivative phenyl-N-tert-butylcarbamate, formed by removal of the urea side chain, which does not affect photosynthesis at concentrations below 10-3M.


1982 ◽  
Vol 85 (1) ◽  
pp. 257-263 ◽  
Author(s):  
A. Graja ◽  
M. Przybylski ◽  
B. Butka ◽  
R. Swietlik

2002 ◽  
Vol 23 (2) ◽  
pp. 125-207 ◽  
Author(s):  
Igor D. Sadekov ◽  
Alexander V. Zakharov ◽  
Alexander A. Maksimenko
Keyword(s):  

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