58150-21-3

Upstream product

• 75526-77-1 (S)-3-[2-(1,1-Dimethyl-allyl)-1H-indol-3-ylmethyl]-1,4-dioxo-octahydro-pyrrolo[1,2-a]pyrazine-3-carboxylic acid 
• 75526-76-0 methyl 3-<2-(1,1-dimethylallyl)indol-3-ylmethyl>-1,4-dioxoperhydropyrrolo<1,2-a>pyrazine-3-carboxylate 
• 57767-78-9 3-<2-(N-benzyloxycarbonyl-L-prolylamido)-2-ethoxycarbonylethyl>-2-(1,1-dimethylallyl)-indole 

Relevant academic research and scientific papers

Studies on the Syntheses of Heterocyclic Compounds. Part 876. The Chiral Total Synthesis of Brevianamide E and Deoxybrevianamide E

The chiral total synthesis of brevianamide E (1) and deoxybrevianamide E (2) starting from L-proline is described.Condensation of 2-(1,1,dimethylallyl)-3-dimethylaminomethylindole (3) and (-)-methyl 1,4-dioxoperhydropyrrolopyrazine-3-carboxylate (7

STUDIES ON INDOLIC MOULD METABOLITES. TOTAL SYNTHESIS OF L-PROLYL-2-METHYLTRYPTOPHAN ANHYDRIDE AND DEOXYBREVIANAMIDE E

Syntheses of L-prolyl-2-methyl-L-tryptophan anhydride, L-prolyl-2-methyl-D-tryptophan anhydride, deoxybrevianamide E, and L-prolyl-2-(1,1-dimethylallyl)-D-tryptophan anhydride are described.A route for the conversion of deoxybrevianamide E into brevianami