Results 191 to 200 of about 4,788 (230)
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Reactions of Benzylamine with Sulfur
Canadian Journal of Chemistry, 1971A five-step sequence has been established for the room temperature reaction of sulfur with benzylamine. Benzylamine polysulfides and benzylidenimine polysulfides occur as interconverting intermediates in this system. The final products are benzylammonium polysulfides, ammonia, and N-benzylidene benzylamine.
Yukihiko Sasaki, Fredric P. Olsen
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Synthesen in der Benzylamin‐Reihe
Justus Liebigs Annalen der Chemie, 1963AbstractDie Darstellung von verschieden substituierten 2‐Amino‐ und 4‐Amino‐3.5‐ dihalogen‐benzylaminen wird beschrieben.
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Oxidation of Benzylamines to Amides
Synthetic Communications, 1997Abstract A convenient method for the conversion of tertiary benzylamines to benzamides by phase transfer oxidation is described. Yields are good. Regioselectivities are reported.
J. Hodge Markgraf +2 more
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Benzylamines: synthesis and evaluation of antimycobacterial properties
Journal of Medicinal Chemistry, 1984The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (19, MIC 10.2 micrograms/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 micrograms/mL), and N-butyl-3,
W R, Meindl +3 more
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Organic & Biomolecular Chemistry, 2016
This work reports the synthesis of quinazolines from 2-aminobenzylamines with N-substituted benzylamines in the presence of molecular iodine. The developed methodology works smoothly under transition-metal free, additive free and solvent free conditions and the use of O2 as a green oxidant makes it a greatly economical.
Abhishek R. Tiwari +1 more
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This work reports the synthesis of quinazolines from 2-aminobenzylamines with N-substituted benzylamines in the presence of molecular iodine. The developed methodology works smoothly under transition-metal free, additive free and solvent free conditions and the use of O2 as a green oxidant makes it a greatly economical.
Abhishek R. Tiwari +1 more
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Journal of Polymer Science Part A: Polymer Chemistry, 1999
The new monomers 3-(3-methacryloxypropoxy)benzylamine and 4-(3-methacryloxypropoxy)benzylamine in the form of hydrochlorides have been synthesized and radically copolymerized under various conditions with comonomers of different hydrophilicity, including N-acryloylmorpholine, N-acryloylpyrrolidine, N,N-dimethylacrylamide, and N-vinylbenzoylmorpholine ...
BERTINI, VINCENZO +5 more
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The new monomers 3-(3-methacryloxypropoxy)benzylamine and 4-(3-methacryloxypropoxy)benzylamine in the form of hydrochlorides have been synthesized and radically copolymerized under various conditions with comonomers of different hydrophilicity, including N-acryloylmorpholine, N-acryloylpyrrolidine, N,N-dimethylacrylamide, and N-vinylbenzoylmorpholine ...
BERTINI, VINCENZO +5 more
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Plasma Benzylamine Oxidase Activity in Cerebrovascular Disease
European Neurology, 1990The plasma benzylamine oxidase level (BzAO) was determined in 60 patients with different types of acute cerebrovascular disease, such as cerebral bleeding, subarachnoid bleeding and cerebral infarction. Patients with cerebral infarction included both apoplectic and multiple types.
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Halogen-substituted benzylamine crown ether inclusion complexes
Acta Crystallographica Section C Structural ChemistryNoncovalent interactions have received much attention in the fields of supramolecular chemistry and crystal engineering. Hydrogen bonding and weak interaction forces affect crystal stacking. Crown-ether-based host–guest inclusion compounds with hydrogen bonding and weak intermolecular interaction forces deserve our attention.
Yan-Juan Wang +3 more
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Catalytic asymmetric α C(sp3)–H addition of benzylamines to aldehydes
Nature Catalysis, 2022Shen Ye, Jing Cao, Baoguo Zhao
exaly

