102720-41-2

Upstream product

• 102720-40-1 1-[3-((2Z,6E)-10-Bromo-11-hydroxy-3,7,11-trimethyl-dodeca-2,6-dienyl)-2,3-dihydro-indol-1-yl]-2,2,2-trifluoro-ethanone 
• 102720-40-1 1-[3-((2E,6E)-10-Bromo-11-hydroxy-3,7,11-trimethyl-dodeca-2,6-dienyl)-2,3-dihydro-indol-1-yl]-2,2,2-trifluoro-ethanone 
• 102720-39-8 2,2,2-Trifluoro-1-[3-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-2,3-dihydro-indol-1-yl]-ethanone 
• 102720-34-3 3-((2E,6E)-3,7,11-Trimethyl-dodeca-2,6,10-trienyl)-2,3-dihydro-1H-indole 
• 102720-33-2 3-(3,7,11-trimethyldodeca-2,6,10-trienyl)-1H-indole 
• 102720-24-1 Indole-3-magnesium iodide 
• 102720-45-6 2,2,2-Trifluoro-1-[3-((2Z,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-2,3-dihydro-indol-1-yl]-ethanone 
• 102720-44-5 3-((2Z,6E)-3,7,11-Trimethyl-dodeca-2,6,10-trienyl)-2,3-dihydro-1H-indole 
• 102779-04-4 3-Z,E-farnesyl indole 
• 24163-93-7 farnesyl bromide 

Relevant academic research and scientific papers

SYNTHESIS OF 3-ω-EPOXIDO FARNESYL INDOLES, INTERMEDIATES IN THE BIOGENESIS OF SESQUITERPENIC INDOLE ALKALOIDS

Epoxides 1a,b, the probable bioprecursors of a serie of indoloterpene alkaloids, were synthesized from indole and farnesyl bromides through application of the Van Tamelen regiospecific epoxidation process to the derived N-acylindolines 14a,b.