imines and 1.35 Å for conjugated imines. By contrast, C-N distances in amines and nitriles are 1.47 and 1.16 Å, respectively. Rotation about the C=N bond...

découverte d'un nouveau principe végétal dans le suc des asperges". Annales de Chimie (in French). 57: 88–93. hdl:2027/nyp.33433062722578. Plimmer RH (1912) [1908]...

used as a surfactant or fabric softener. Methylation to create a tertiary amine is illustrated as: CH3(C6H4)NH2 + (CH3O)2SO2 (in NaHCO3 aq) → CH3(C6H4)N(CH3)2...

that the amino acid glycine—which was then called glycocolle—might be the amine of a hypothetical acid, which he called "glycolic acid" (acide glycolique)...

le camphoryle" [On pinic and sylvic acids, and on camphoryl]. Annales de Chimie et de Physique. 2nd series (in French). 65: 324–332.; see "Camphoryle",...

specifically with primary amines above their isoelectric point Pi in presence of thiols. OPA reacts also with thiols in presence of an amine such as n-propylamine...

amines and triazoles. Tertiary amines can react with DCM to form quaternary chloromethyl chloride salts via the Menshutkin reaction. Secondary amines...

share the same functional group, a carbonyl group attached to two organic amine residues: R1R2N−C(=O)−NR3R4, where R1, R2, R3 and R4 groups are hydrogen...

(Part 1): CHEMICAL AND PHARMACOLOGICAL PROPERTIES". Journal Marocain de Chimie Hétérocyclique. 16 (1): 1–47. ISSN 1114-7792. Retrieved July 3, 2017. Raimund...

(RC(CCl3)=NH) in the Houben-Fischer synthesis Nitriles can be obtained from primary amines via oxidation. Common methods include the use of potassium persulfate,...