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Usage

Uses

Used in Pharmaceutical Industry:
1-Acetyl-3,5-dimethyl Adamantane is used as a starting material for the synthesis of new pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of innovative drugs with potential therapeutic applications.
Used in Agricultural Industry:
1-Acetyl-3,5-dimethyl Adamantane is also used as a starting material for the synthesis of new agrochemical compounds. Its properties and structure contribute to the creation of effective pesticides and other agricultural chemicals, enhancing crop protection and yield.

Upstream product

• 702-79-4 1,3-dimethyladamantane 
• 431-03-8 dimethylglyoxal 
• 26919-42-6 (3,5-dimethyl-adamantan-1-yl)-methanol 
• 14670-94-1 3,5-dimethyl-1-adamantanecarboxylic acid 
• 917-54-4 methyllithium 

Downstream Products

• 19982-08-2 memantine* 
• 41100-52-1 memantine hydrochloride 

Relevant academic research and scientific papers

Enantioselective borohydride reduction of aliphatic ketones catalyzed by ketoiminatocobalt(iii) complex with 1-chlorovinyl axial ligand

For the enantioselective borohydride reduction of aliphatic ketones, the optically active ketoiminatocobalt(II) catalysts was successfully designed based on their axial ligand. Instead of chloroform for the aryl ketone reduction, various axial ligand precursors were examined for the aliphatic ketone. Consequently, 1, 1, 1-trichloroethane was found to be the most effective activator of the cobalt(II) complexes to generate the corresponding 1-chlorovinyl cobalt(III) derivatives as the reactive intermediate. Several aliphatic ketones were successfully reduced to afford the corresponding secondary alcohols with high enantioselectivities.

Methods of acylating adamantane, tricyclo[5.2.1.02,6], and decalin compounds

An acylating agent of the invention includes (A) a 1,2-dicarbonyl compound or its hydroxy reductant, (B) oxygen, and (C) at least one compound selected from (c1) a metallic compound and (C2) N-hydroxyphthalimide or another imide compound. As the 1,2-dicarbonyl compound or its hydroxy reductant (A), biacetyl, 2,3-butanediolor the like canbeused. As the metallic compound (c1), cobalt acetate, or another cobalt compound, for example, can be employed. By reacting an adamantane derivative or another compound having a methine carbon atom with the acylating agent, an acyl group can be introduced to the methine carbon atom with efficiency.