263368-66-7

Upstream product

• 61589-86-4 3-(3-hydroxy-propyl)cyclohex-2-en-1-one 
• 80206-58-2 Toluene-4-sulfonic acid 3-(3-hydroxy-cyclohex-1-enyl)-propyl ester 
• 263368-52-1 Toluene-4-sulfonic acid 3-(3-oxo-cyclohex-1-enyl)-propyl ester 
• 263368-55-4 Acetic acid 3-[3-(toluene-4-sulfonyloxy)-propyl]-cyclohex-2-enyl ester 

Downstream Products

• 263368-45-2 3-{3-[(2-Benzo[1,3]dioxol-5-yl)ethylamino]propyl}cyclohex-2-enyl acetate 

Relevant academic research and scientific papers

Palladium-catalyzed synthesis of cephalotaxine analogues

The synthesis of cephalotaxine ring analogues 10 was achieved by two successive intramolecular palladium-catalyzed reactions of 12 via 11, namely an allylic amination and a Heck reaction. The substrates 12 were obtained by alkylation of primary amines 13 with tosylates 14.