60196-90-9

Usage

InChI:InChI=1/C13H23N/c1-2-12(14)13-6-9-3-10(7-13)5-11(4-9)8-13/h9-12H,2-8,14H2,1H3/p+1/t9?,10?,11?,12-,13?/m1/s1

Upstream product

• 23074-42-2 1-adamantanecarbonitrile 
• 75-03-6 ethyl iodide 
• 768-93-4 1-iodoadamantane 
• 26525-23-5 Ethyl-<1>adamantyl-keton-oxim 

Downstream Products

• 366-18-7 [2,2]bipyridinyl 
• 1283234-48-9 N-[1-(1-adamantyl)propyl]-4-chloroaniline 
• 106-47-8 4-chloro-aniline 
• 1283234-49-0 N-[1-(1-adamantyl)propyl]-3-chloroaniline 
• 1283234-50-3 N-[1-(1-adamantyl)propyl]-2-chloroaniline 
• 1660-05-5 1-(adamantan-1-yl)propan-1-one 
• 1283234-26-3 C₁₉H₂₇N 
• 1283234-52-5 N-[1-(1-adamantyl)propyl]-3-bromoaniline 
• 1283234-55-8 N,N'-bis[1-(1-adamantyl)propyl]benzene-1,3-diamine 
• 1283234-51-4 N-[1-(1-adamantyl)propyl]-4-bromoaniline 
• 106-40-1 4-bromo-aniline 
• 1283234-54-7 N,N'-bis[1-(1-adamantyl)propyl]benzene-1,4-diamine 
• 1283234-53-6 N-[1-(1-adamantyl)propyl]-2-bromoaniline 

Relevant academic research and scientific papers

Nickel-Catalyzed C-Alkylation of Nitroalkanes with Unactivated Alkyl Iodides

Enabled by nickel catalysis, a mild and general catalytic method for C-alkylation of nitroalkanes with unactivated alkyl iodides is described. Compatible with primary, secondary, and tertiary alkyl iodides; and tolerant of a wide range of functional groups, this method allows rapid access to diverse nitroalkanes.

Synthesis of a new family of adamantylpyridin-2-amines by palladium-catalyzed amination

Palladium-catalyzed arylation of various adamantane-containing amines with 2-bromopyridine has been studied, and the influence of the phosphane ligand, concentration, and molar ratio of the reagents on the composition of the reaction mixture and on the yield of the target adamantylpyridin-2-amines has been analyzed. The dependence of the formation of N,N-diarylated products on the nature of the starting adamantylamines is shown. Georg Thieme Verlag Stuttgart.