1726-86-9Relevant articles and documents
Cytokinin receptor antagonists derived from 6-benzylaminopurine
Nisler, Jaroslav,Zatloukal, Marek,Popa, Igor,Dole?al, Karel,Strnad, Miroslav,Spíchal, Luká?
body text, p. 823 - 830 (2010/07/04)
Recently we reported 6-(2-hydroxy-3-methylbenzylamino)purine (PI-55) as the first molecule to antagonize cytokinin activity at the receptor level. Here we report the synthesis and in vitro biological testing of eleven BAP derivatives substituted in the be
SUBSTITUTED PYRIMIDINES
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Page/Page column 25, (2008/06/13)
The invention relates to novel substituted pyrimidines of formula (I), in which R1, R2, R3, R4, Q, X and n have the meanings as cited in the description. The invention also relates to a method and intermediate products for producing these pyrimidines, and to the use thereof as plant control agents, particularly as herbicides.
Magnesium-mediated ortho-Specific Formylation and Formaldoximation of Phenols
Aldred, Robert,Johnston, Robert,Levin, Daniel,Neilan, James
, p. 1823 - 1832 (2007/10/02)
Deprotonation of phenols using magnesium methoxide, followed by distillative removal of free methanol and addition of paraformaldehyde results in ortho-specific magnesium mediated formylation to give the corresponding salicyladehyde magnesium salts, from which the salicylaldehydes can be isolated by acidic work-up.Addition of aq. hydroxylamine sulfate to the salicylaldehyde magnesium salt, in place of the acid work-up, gives the corresponding salicylaldoximes.
