Results 211 to 220 of about 60,877 (255)
Some of the next articles are maybe not open access.
Unusual Nitrile–Nitrile and Nitrile–Alkyne Coupling of FcCN and FcCCCN
Chemistry – A European Journal, 2014AbstractInvited for the cover of this issue is the group of Uwe Rosenthal at Leibniz Institute for Catalysis (LIKAT Rostock) and the group of Heinrich Lang at the Technische Universität Chemnitz. The image depicts five coupling possibilities of alkynes and nitriles at metallocenes. Read the full text of the article at 10.1002/chem.201304478.
Frank Strehler +7 more
openaire +3 more sources
Nitrile Ylide Dimerization: Investigation of the Carbene Reactivity of Nitrile Ylides
The Journal of Organic Chemistry, 2004A series of novel hexaaryl diazatrienes 5 ("nitrile ylide dimers") were synthesized directly from the corresponding diaryl ketimines 12 and dichlorotoluenes 13 in a facile one-pot synthesis. The carbene character of the nitrile ylides was investigated by varying the substituents on the aromatic ring adjacent to the carbene center.
Stephen Eustace +2 more
openaire +3 more sources
Reactivity of Coordinated Nitriles
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
V. Yu. Kukushkin, Armando J. L. Pombeiro
openaire +3 more sources
Activation of nitriles by hydrogen bonding in cycloadditions with nitrile oxides
Journal of Heterocyclic Chemistry, 1984AbstractThe dipolarophilic activity of aromatic nitriles in cycloaddition with benzonitrile oxides is remarkably enhanced by ortho‐acylamino substituents. The activation depends upon the solvent and can be ascribed to a hydrogen bond which assists cycloaddition.
Antonino Corsaro +3 more
openaire +2 more sources
ChemInform Abstract: Enantioselective Biotransformation of Nitriles
ChemInform, 2011AbstractReview: 52 refs.
Mei-Xiang Wang, Mei-Xiang Wang
openaire +3 more sources
N‐Substituted Nitriles and Other Hetero Analogues of Nitriles of the Type RCZ
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Santiago Vázquez, Carmen Escolano
openaire +2 more sources
Dienaminoboranes and their reaction with nitriles
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1976AbstractDurch exotherme Umsetzung von Allyl‐dialkylboranen (I) mit Nitrilen (II) bei ‐60°C erhält man die Iminoborane (III), die sich zu den Boranen (IV) isomerisieren.
Yu. N. Bubnov +2 more
openaire +3 more sources
Generation, Identification, and Synthetic Applications of Nitrile Sulfides and Nitrile Selenides
Current Organic Chemistry, 2011AbstractReview: 78 refs.
Melinda Krebsz, Tibor Pasinszki
openaire +3 more sources
2001
Cyanides are among the most acutely toxic of all industrial chemicals and are produced in large quantities and used in many different applications. However, they cause few serious accidents or deaths. This is partly because the word cyanide is synonymous with a highly poisonous substance and a certain amount of care in handling is thereby ensured.
openaire +2 more sources
Cyanides are among the most acutely toxic of all industrial chemicals and are produced in large quantities and used in many different applications. However, they cause few serious accidents or deaths. This is partly because the word cyanide is synonymous with a highly poisonous substance and a certain amount of care in handling is thereby ensured.
openaire +2 more sources
Chemical Reviews, 1948