91086-12-3Relevant academic research and scientific papers
Synthesis of Cyanamides from Cyanogen Bromide under Mild Conditions through N-Cyanation of Allylic Tertiary Amines
Liang, Honggang,Bao, Lingxiang,Du, Yao,Zhang, Yiying,Pang, Siping,Sun, Chenghui
supporting information, p. 2675 - 2679 (2017/10/06)
Cyanamides were selectively formed through a one-step nucleophilic substitution reaction of allylic tertiary amines with cyanogen bromide. Because of the mild reaction conditions and good yields of the reaction, as well as the commercial availability of the starting materials, this new method represents a valuable tool for the synthesis of cyan-amides through an N-deallylation reaction and an N-cyanation reaction in one pot.
METATHESIS CATALYSTS CONTAINING ONIUM GROUPS
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Page/Page column 67, (2013/09/12)
Disclosed herein is a general method for the preparation of complexes containing a quaternary onium group in an inert ligand. Some of these complexes may be represented by formula (1): Methods for the preparation of complexes of formula 1, the preparation
Zinc mediated alkylation of cyclic secondary amines
Murty,Jyothirmai,Krishna, Palakodety Radha,Yadav
, p. 2483 - 2486 (2007/10/03)
Zinc metal mediated simple and efficient alkylation of cyclic secondary amines e.g., piperazines and morpholine with allyl bromide, chlorobromo propane and p-methoxy benzyl bromide is described in good yields.
