93264-60-9

Upstream product

• 501-53-1 benzyl chloroformate 
• 93264-58-5 5-(2-Methyl-[1,3]dioxolan-2-yl)-2H-pyridine-1-carboxylic acid benzyl ester 
• 55676-25-0 3-(2-methyl-[1,3]dioxolan-2-yl)-pyridine 
• 93264-59-6 (3R,6R)-3-Hydroxy-6-(1H-indol-3-yl)-5-(2-methyl-[1,3]dioxolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 

Downstream Products

• 93264-61-0 5-Acetyl-6-(1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 93264-64-3 (2R,3R)-3-Acetyl-3-ethyl-2-(1H-indol-3-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 93264-62-1 5-Acetyl-6-[1-(1-ethoxy-ethyl)-1H-indol-3-yl]-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 93264-65-4 3-((2R,3R)-3-Acetyl-1-benzyloxycarbonyl-3-ethyl-1,2,3,6-tetrahydro-pyridin-2-yl)-indole-1-carboxylic acid methyl ester 
• 93264-63-2 (2R,3R)-3-Acetyl-2-[1-(1-ethoxy-ethyl)-1H-indol-3-yl]-3-ethyl-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 102327-24-2 (2S,3S)-3-Acetyl-2-(1H-indol-3-yl)-piperidine-1-carboxylic acid benzyl ester 
• 102327-23-1 (2S,3R,5R)-3-Acetyl-2-(1H-indol-3-yl)-5-(2-methoxy-ethoxymethoxy)-piperidine-1-carboxylic acid benzyl ester 
• 102327-22-0 (2S,3R,5R)-3-Acetyl-5-benzoyloxy-2-(1H-indol-3-yl)-piperidine-1-carboxylic acid benzyl ester 
• 102349-08-6 (2S,3R,5R)-3-Acetyl-5-(1-ethoxy-ethoxy)-2-(1H-indol-3-yl)-piperidine-1-carboxylic acid benzyl ester 
• 102327-19-5 Benzoic acid (3S,5S,6R)-5-acetyl-1-(2-hydroxy-ethyl)-6-(1H-indol-3-yl)-piperidin-3-yl ester 
• 102327-18-4 Benzoic acid (3S,5S,6R)-5-acetyl-6-(1H-indol-3-yl)-piperidin-3-yl ester 
• 102327-24-2 (2S,3R)-3-Acetyl-2-(1H-indol-3-yl)-piperidine-1-carboxylic acid benzyl ester 
• 102327-15-1 (2S,3R,5R)-3-Acetyl-5-hydroxy-2-(1H-indol-3-yl)-piperidine-1-carboxylic acid benzyl ester 
• 102327-14-0 (3R,6R)-5-Acetyl-6-(1H-indol-3-yl)-3-methanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

A NEW SYNTHETIC METHOD FOR THE FRAMEWORK OF ASPIDOSPERMA ALKALOIDS USING SINGLET OXYGEN CHEMISTRY

A singlet oxygen adduct of 1-benzyloxycarbonyl-1,2-dihydro-5-(2-methyl-1,3-dioxolan-2-yl)pyridine (21) was treated with indole in the presence of stannous chloride to yield directly the complex compound 22, which will act as a suitable starting material f

A NEW SYNTHESIS OF (+/-)-VINDOROSINE

The pentacyclic compound (15) was stereoselectively synthesized in the racemic form using indole and acetylpyridine as starting materials according to the synthetic route shown in Chart. 2.This constitutes a new formal synthesis of (+/-)-vindorosine (16).