929296-01-5

Upstream product

• 929295-93-2 acetic acid 1-cyclohex-1-enyl-2-(3-hydroxy-propyl)-allyl ester 
• 929295-97-6 acetic acid 2-(3-azido-propyl)-1-cyclohex-1-enyl-allyl ester 
• 929295-89-6 acetic acid 2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-1-cyclohex-1-enyl-allyl ester 
• 120001-35-6 ((4-bromopent-4-en-1-yl)oxy)(tert-butyl)dimethylsilane 
• 64180-78-5 4-bromopent-4-en-1-ol 
• 929295-85-2 2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-1-cyclohex-1-enyl-prop-2-en-1-ol 
• 936747-30-7 2-(3-azido-propyl)-1-cyclohex-1-enyl-prop-2-en-1-ol 

Relevant academic research and scientific papers

Intramolecular azide trapping of the Nazarov intermediate: Formation of peroxy-bridged indolizidinones via a deep-seated rearrangement and aerobic oxidation

Cross-conjugated dienones with pendent azide side chains undergo interrupted Nazarov trapping, leading to peroxy-bridged indolizidinones in good yields. This process is proposed to involve skeletal rearrangement of the initial trapping product, with loss