Results 71 to 80 of about 128 (98)
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Chemischer Informationsdienst, 1978
AbstractDie Behandlung des Mo‐Komplexes (III) mit den Amidinen (II) führt zu den Amidinato‐Komplexen (I).
Brunner, Henri, Wachter, Joachim
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AbstractDie Behandlung des Mo‐Komplexes (III) mit den Amidinen (II) führt zu den Amidinato‐Komplexen (I).
Brunner, Henri, Wachter, Joachim
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ChemInform Abstract: Chiral Cyclic Amidines.
ChemInform, 1994AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Hans Wynberg, W. Ten Hoeve
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Aminooxazolinate — A Chiral Amidinate Analogue.
ChemInform, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
Ian J. Munslow +3 more
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Facile N-arylation of amidines and N,N-disubstituted amidines [PDF]
Tetrahedron Letters, 2015 AbstractA facile procedure for the reaction of amidines with in situ generated arynes to form N‐arylated amidines is presented.
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Amidine- and amidinate-functionalised N-heterocyclic carbene complexes of silver and chromium
Dalton Transactions, 2012A new family of N,N'-bis-(2,6-diisopropylphenyl)-(2,6-diisopropylphenyl-imidazolium)-acetamidines have been developed as NHC proligands and ligands that are functionalised with neutral amidine and anionic amidinato moieties. On coordination they adopt diverse binding modes, depending on the nature of the metal and the reaction conditions.
Robert P. Tooze +4 more
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Fresenius' Zeitschrift f�r Analytische Chemie, 1960
The polarographic properties of some aliphatic, arylaliphatic, phenoxyaliphatic and aromatic amidines have been investigated. Aliphatic and arylaliphatic amidines are not reducible in the range 0 to −1.8 volts versus the saturated calomel electrode. Phenoxyacetamidines are reduced to the phenol and acetamidine.
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The polarographic properties of some aliphatic, arylaliphatic, phenoxyaliphatic and aromatic amidines have been investigated. Aliphatic and arylaliphatic amidines are not reducible in the range 0 to −1.8 volts versus the saturated calomel electrode. Phenoxyacetamidines are reduced to the phenol and acetamidine.
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Molecular Recognition of Amidines in Water
Organic Letters, 2003[structure: see text] Tetraphosphonates of the general structure shown above are biomimetic hosts for bisamidinium cations in drugs such as pentamidine and DAPI. Similar to their insertion into DNA's minor groove, these drugs are often sandwiched by two tetraphosphonate hosts (2:1). The alternative binding mode (1:2) produces extremely high association
Grawe, Thomas +2 more
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Mono-amidinate complexes stabilized by a new sterically-hindered amidine†
Chemical Communications, 1999A novel amidinate ligand incorporating a bulky terphenyl group is used to prepare unusual, low-coordinate lithium and yttrium mono-amidinate complexes.
Joseph A. R. Schmidt, John Arnold
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Amidination of Lysine Side Chains
ChemInform, 1996AbstractFor Abstract see ChemInform Abstract in Full Text.
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Reactions with heterocyclic amidines 1. Cyanoethylation of cyclic amidines
Journal of Heterocyclic Chemistry, 1978Abstract2‐Amino‐5‐phenyl‐1,3,4‐oxadiazole (1a) and 2‐amino‐1,3,4‐thiadiazole (1b) reacted with acrylonitrile to yield β‐cyanoethylamino derivatives. On the other hand, 2‐amino‐4‐phenylthiazole (2) reacted with acrylonitrile under the same experimental conditions to yield a di‐β‐cyanoethylaminothiazole derivative.
Mohamed Hilmy Elnagdi +3 more
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