615537-72-9

Upstream product

• 52488-36-5 4-bromo-1H-indole 
• 52133-67-2 ethyl 2-cyano-4,4-diethoxybutyrate 
• 615537-82-1 2-(aminomethyl)-4,4-diethoxy-1-butanol 
• 151726-06-6 4-bromo-3-(2-oxoethyl)-1H-indole-1-carboxylic acid 1,1-dimethylethyl ester 
• 615537-71-8 N-[2-(tert-butyldiphenylsilyloxymethyl)-3-butenyl]-N-methylamine 
• 615537-84-3 tert-butyl N-[2-(tert-butyldiphenylsilyloxymethyl)-4,4-diethoxybutyl]carbamate 
• 615537-86-5 tert-butyl N-[2-(tert-butyl-diphenylsilyloxymethyl)-4,4-diethoxybutyl]-N-methylcarbamate 
• 615537-88-7 tert-butyl N-[4-bromo-2-(tert-butyl-diphenylsilyloxymethyl)butyl]-N-methylcarbamate 
• 615537-87-6 tert-butyl N-[2-(tert-butyl-diphenylsilyloxymethyl)-4-hydroxybutyl]-N-methylcarbamate 
• 615537-89-8 tert-butyl N-[2-(tert-butyldiphenylsilyloxymethyl)-3-butenyl]-N-methylcarbamate 
• 151726-05-5 4-bromo-3-cyanomethyl-1H-indole-1-carboxylic acid 1,1-dimethylethyl ester 
• 89245-35-2 2-(4-bromo-1H-indol-3-yl)acetonitrile 
• 24424-99-5 di-tert-butyl dicarbonate 

Relevant academic research and scientific papers

seco-C/D Ring Analogues of Ergot Alkaloids. Synthesis via Intramolecular Heck and Ring-Closing Metathesis Reactions

Equation presented. Intramolecular Heck and ring-closing metathesis reactions on key intermediates 10 and 15, respectively, provide efficient entries into seco-C/D ring analogues of Ergot alkaloids 12 and 16, compounds of potential synthetic and biologica