13679-88-4Relevant academic research and scientific papers
Electrochemical oxidative annulation of amines and aldehydes or ketones to synthesize polysubstituted pyrroles
Gao, Xinlong,Wang, Pan,Wang, Qingqing,Chen, Jingting,Lei, Aiwen
supporting information, p. 4941 - 4945 (2019/09/30)
A general and practical protocol to synthesize polysubstituted pyrroles has been established by electrooxidative annulation of amines and aldehydes or ketones. In an undivided cell, arylacetaldehydes and primary amines can participate in this transformati
First efficient two-step/one-pot zirconium (IV)isopropoxide-mediated reductive amination of carbonyl compounds
Pieri, Cyril,Brunel, Jean Michel
, p. 448 - 456 (2015/06/22)
An efficient method for the synthesis of various primary and secondary amines through a zirconium(IV) isopropoxide-mediated reductive amination reaction of aldehydes and ketones is reported. A series of different aldehydes, ketones and amines were used leading to the expected amino products in moderate to excellent yields. The mechanistic rationale of this reaction has been postulated through the formation of a transient imine species and a diastereoselective version using (R)-phenylethylamine as chiral inducer led to the expected products in moderate to excellent yields and with diastereoselectivities up to 100%.
Synthesis and Herbicidal Activity of N-(1-Arylethenyl)-2-chloroacetamides
Okamoto, Hidenori,Kato, Shozo,Ogasawara, Masaru,Konnai, Makoto,Takematsu, Tetsuo
, p. 2733 - 2736 (2007/10/02)
N-(1-Alkenyl)-2-chloroacetamides, which bear an aryl substituent at the 1-position of the alkenyl moiety, were synthesized and their herbicidal activities were tested.Some of them were active against paddy field weeds.In particular, a new type of chloroac
