144876-97-1Relevant articles and documents
HERBICIDAL CINNOLINIUM COMPOUNDS
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Page/Page column 77-78, (2020/07/14)
Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially as herbicides.
N-(heterocyclyl)benzene or pyridinesulphonamides as antithrombotic agents and anticoagulants
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, (2008/06/13)
Compounds of formula [I] in which: W may represent a —(CH2)2—, —(CH2)3—, —CH2—C≡C— or —CH2—CH═CH— group, R2 may in particular represent a piperidyl group, an optionally substituted 1,2,3,6-tetrahydropyridyl group, a hexahydro-1H-azepinyl group, an optionally substituted piperazinyl group or a morpholinyl group, R3 may in particular represent a group —COR1, A may in particular represent an optionally substituted phenyl group, a heterocycle or a cyclopentyl group, and B may in particular represent a pyridyl group, an aminopyrazinyl group, an aminopyridazinyl group, a pyrimidinyl group optionally substituted with an amino group, piperidyl group or an aminopyridyl group optionally substituted on the pyridine with a (C1-C4)alkyl or (C1-C4)alkoxy group, the amino group possibly also being substituted with a (C1-C4)alkyl group, their preparation and their therapeutic application.
Synthesis of Two Stable Nitrogen Analogues of S-Adenosyl-L-methionine
Thompson, Mark J.,Mekhalfia, Abdelaziz,Hornby, David P.,Blackburn, G. Michael
, p. 7467 - 7473 (2007/10/03)
Homochiral syntheses of two stable nitrogen analogues of S-adenosyl-L-methionine (AdoMet) are described. In the first analogue, AzaAdoMet, the sulfonium center of AdoMet, is replaced by an N-methyl moiety whose pKa is 7.08. This provides a char
Preparation of amino- and carboxy-protected L-α-amino-ω-iodocarboxylic acids
Easmon,Heinisch,Holzer,Matuszczak
, p. 367 - 370 (2007/10/02)
The synthesis of L-α-amino-ω-iodobutyric, valeric, and caproic acid esters protected at the amino function by a benzyloxycarbonyl group is reported.
