145801-29-2

Upstream product

• 18172-67-3 beta-pinene 
• 79559-56-1 (+)-makomakine 
• 145801-26-9 (1R,4R,5S,7R)-4-[1-(4-Methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2-dimethyl-6-methylene-3-aza-bicyclo[3.3.1]nonan-7-ol 
• 159979-20-1 (1S,4R,5R,6S)-6-Hydroxymethyl-4-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2-dimethyl-3-aza-bicyclo[3.3.1]nonan-6-ol 
• 159979-18-7 N⁽¹⁾-p-methoxyphenylsulfonylmakomakine 
• 159979-24-5 Acetic acid (1S,4R,5R,6S)-6-hydroxy-4-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2-dimethyl-3-aza-bicyclo[3.3.1]non-6-ylmethyl ester 
• 145801-28-1 (1S,4R,5S)-6-Chloromethyl-4-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2-dimethyl-3-aza-bicyclo[3.3.1]non-6-ene 
• 127-08-2 potassium acetate 

Downstream Products

• 145801-30-5 {(1S,4R,5S)-4-[1-(4-Methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2-dimethyl-3-aza-bicyclo[3.3.1]non-6-en-6-yl}-methanol 

Relevant academic research and scientific papers

Synthesis of Aristotelia-Type alkaloids. Part XIV. Total synthesis of (+)-Aristolone

The first total synthesis of the highly functionalized monoterpenoid indole alkaloid (+)-aristolone ((+)-2) is described. This investigation uncovered the hitherto unknown relative and absolute configuration of this rare metabolite which had been isolated

Synthesis of Aristotelia-type alkaloids. Part XI. Total synthesis of (+)-sorelline and (+)-aristolasene

Optically pure samples of the rare Aristotelia alkaloids (+)-sorelline (2) and (+)-aristolasene (3) have been synthesized for the first time. Since natural (S)-perilla alcohol served as one of the starting building blocks, these syntheses delineate the pr