744203-14-3

Upstream product

• 1604-29-1 1,1-dimethyl-2-propynyl acetate 
• 2717-76-2 (S)-N-benzyloxycarbonyl-L-tryptophan methyl ester 
• 7432-21-5 N-carbobenzyloxy-L-tryptophane 
• 744203-12-1 methyl (2S,4RS)-2-benzyloxycarbonylamino-3-(2,3-dihydro-1H-indol-3-yl)propionate 
• 744203-13-2 2-benzyloxycarbonylamino-3-[1-(1,1-dimethyl-prop-2-ynyl)-2,3-dihydro-1H-indol-3-yl]-propionic acid methyl ester 

Relevant academic research and scientific papers

A general synthesis of N-reverse-prenyl indoles

A general method for the construction of N-reverse-prenyl indoles was established using copper catalyzed N-propargylation, the Lindlar hydrogenation of the acetylenic bond, and dehydrogenation with chemical manganese dioxide as key steps. The antifungal i

Synthetic studies of N-reverse prenylated indole. An efficient synthesis of antifungal indole alkaloids and N-reverse prenylated tryptophan

The efficient method for the synthesis of N-1,1-dimethyl-2-propenyl (reverse prenyl) indole was developed by the N-propargylation of the indoline, partial hydrogenation of the terminal alkyne, and oxidation to the indole using chemical manganese dioxide (