102673-36-9

Upstream product

• 15590-62-2 lithium 2-ethylhexanoate 
• 100-39-0 benzyl bromide 
• 96648-92-9 (4aR^*,5S^*,6S^*,7S^*)-2-benzyl-7-((2'-ethylhexanoyl)oxy)-3,4,4a,5,6,7-hexahydro-6-hydroxy-5-((methoxymethoxy)methyl)-1(2H)-isoquinolone 
• 96648-91-8 (4aR^*,5S^*,6S^*,7R^*)-2-benzyl-3,4,4a,5,6,7-hexahydro-5-((methoxymethoxy)methyl)-6,7-oxy-1(2H)-isoquinolone 
• 186581-53-3 diazomethane 
• 109961-04-8 (4aR^*,5S^*,6S^*,7S^*)-2-benzyl-6-(benzyloxy)-5-carboxy-7-((2'-ethylhexanoyl)oxy)-3,4,4a,5,6,7-hexahydro-1(2H)-isoquinolone 
• 96648-90-7 (4aR^*,5S^*)-2-benzyl-5-((methoxymethoxy)methyl)-3,4,4a,5-tetrahydro-1(2H)-isoquinolone 
• 102673-37-0 (4aR^*,5S^*,6S^*,7S^*)-2-benzyl-6-(benzyloxy)-7-((2'-ethylhexanoyl)oxy)-3,4,4a,5,6,7-hexahydro-5-((methoxymethoxy)methyl)-1(2H)-isoquinolone 
• 109961-03-7 (4aR^*,5S^*,6S^*,7S^*)-2-benzyl-6-(benzyloxy)-7-((2'-ethylhexanoyl)oxy)-3,4,4a,5,6,7-hexahydro-5-(hydroxymethyl)-1(2H)-isoquinolone 

Downstream Products

• 102673-34-7 (4aS,5R,6R)-6-Acetoxy-2-benzyl-1,2,3,4,4a,5,6,7-octahydro-isoquinoline-5-carboxylic acid methyl ester 
• 4109-62-0 (+/-)-19,20-dehydro-α-yohimbine 
• 109961-22-0 (4aR^*,5S^*,6S^*,8aR^*)-6-acetoxy-2-benzyl-5-(methoxycarbonyl)perhydroisoquinoline 
• 102673-35-8 (4aR^*,5S^*,6S^*,7S^*)-2-benzyl-6-(benzyloxy)-7-((2'-ethylhexanoyl)oxy)-5-(methoxycarbonyl)-1,2,3,4,4a,5,6,7-octahydroisoquinoline 

Relevant academic research and scientific papers

Genaral Strategies for the Synthesis of Indole Alkaloids. Total Syntheses of (+/-)-Reserpine and (+/-)-α-Yohimbine

The concise, total syntheses of the indole alkaloids (+/-)-reserpine (1) and (+/-)-α-yohimbine (4) have been completed by the application of a general strategy that features an intramolecular Diels-Alder reaction for the facile construction of the functio

TOTAL SYNTHESIS OF α-YOHIMBINE

A facile total synthesis of the indole alkaloid α-yohimbine (1) from the hydroisoquinoline derivative 5 has been completed.