109961-01-5

Upstream product

• 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 
• 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 
• 96648-93-0 (4aR^*,5S^*,6S^*,7S^*)-2-benzyl-7-((2'-ethylhexanoyl)oxy)-3,4,4a,5,6,7-hexahydro-6-methoxy-5-((methoxymethoxy)methyl)-1(2H)-isoquinolone 
• 96648-94-1 (4aR^*,5S^*,6S^*,7S^*,8aS^*)-2-benzyl-7-((2'-ethylhexanoyl)oxy)-6-methoxy-5-((methoxymethoxy)methyl)-3,4,4a,5,6,7,8,8a-octahydro-1(2H)-isoquinolone 
• 96648-90-7 (4aR^*,5S^*)-2-benzyl-5-((methoxymethoxy)methyl)-3,4,4a,5-tetrahydro-1(2H)-isoquinolone 
• 109961-00-4 (4aR^*,5S^*,6S^*,7S^*,8aS^*)-2-benzyl-7-((2'-ethylhexanoyl)oxy)-5-hydroxymethyl-6-methoxy-3,4,4a,5,6,7,8,8a-octahydro-1(2H)-isoquinolone 

Downstream Products

• 16625-53-9 2,3-seco-2,3-dihydroreserpine 
• 96648-96-3 (4aR^*,5S^*,6S^*,7S^*,8aR^*)-2-benzyl-6-methoxy-5-(methoxycarbonyl)-7-((3,4,5-trimethoxybenzoyl)oxy)perhydroisoquinoline 
• 109961-17-3 (4aR^*,5S^*,6S^*,7S^*,8aS^*)-2-benzyl-7-((2'-ethylhexanoyl)oxy)-6-methoxy-5-(methoxycarbonyl)perhydroisoquinoline 
• 70617-03-7 (4aR^*,5S^*,6S^*,7S^*,8aR^*)-6-methoxy-5-(methoxycarbonyl)-7-((3,4,5-trimethoxybenzoyl)oxy)perhydroisoquinoline 
• 109961-18-4 (4aR^*,5S^*,6S^*,7S^*,8aR^*)-2-benzyl-7-hydroxy-6-methoxy-5-(methoxycarbonyl)perhydroisoquinoline 
• 109961-20-8 (+/-)-inside reserpine 
• 109961-20-8 (+/-)-inside 3-isoreserpine 
• 50-55-5 (+/-)-reserpine 
• 50-55-5 (+/-)-3-isoreserpine 
• 96648-95-2 (4aR^*,5S^*,6S^*,7S^*,8aS^*)-2-benzyl-7-((2'-ethylhexanoyl)oxy)-6-methoxy-5-(methoxycarbonyl)-3,4,4a,5,6,7,8,8a-octahydro-1(2H)-isoquinolone 

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