383863-70-5

Upstream product

• 24850-33-7 allyltributylstanane 
• 383863-69-2 (3aR,4R,5S,5aS,8aR,8bR)-4-Iodo-7-methoxy-5-[4-(4-methoxy-benzyloxy)-butyl]-2-oxo-decahydro-furo[3,2-e]indole-6-carboxylic acid methyl ester 
• 177977-02-5 C₃₆H₄₅NO₅S₂ 
• 177977-03-6 (4R,5S)-3-{(1R,2R,4aS,8aR)-2-[4-(4-Methoxy-benzyloxy)-butyl]-6-oxo-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carbonyl}-4-methyl-5-phenyl-oxazolidin-2-one 
• 383863-68-1 (3aR,4R,5S,5aS,8aR,8bR)-7-Hydroxy-4-iodo-5-[4-(4-methoxy-benzyloxy)-butyl]-2-oxo-decahydro-furo[3,2-e]indole-6-carboxylic acid methyl ester 
• 177977-05-8 {(1R,2R,4aS,8aR)-2-[4-(4-Methoxy-benzyloxy)-butyl]-6-oxo-1,2,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl}-carbamic acid methyl ester 
• 177977-04-7 (1R,2R,4aS,8aR)-2-[4-(4-Methoxy-benzyloxy)-butyl]-6-oxo-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid 
• 177977-14-9 (1R,2R,4aS,8aR)-2-[4-(4-Methoxy-benzyloxy)-butyl]-6-oxo-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carbaldehyde 
• 177976-99-7 (4R,5S)-3-((E)-5-{2-[(2E,4E)-9-(4-Methoxy-benzyloxy)-nona-2,4-dienyl]-[1,3]dithian-2-yl}-pent-2-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one 
• 383863-66-9 2-(3-{2-[(2E,4E)-9-(4-Methoxy-benzyloxy)-nona-2,4-dienyl]-[1,3]dithian-2-yl}-propoxy)-tetrahydro-pyran 
• 177977-01-4 3-{2-[(2E,4E)-9-(4-Methoxy-benzyloxy)-nona-2,4-dienyl]-[1,3]dithian-2-yl}-propan-1-ol 
• 177977-12-7 3-{2-[(2E,4E)-9-(4-Methoxy-benzyloxy)-nona-2,4-dienyl]-[1,3]dithian-2-yl}-propionaldehyde 
• 177977-20-7 ethyl (2E,4E)-9-(4-methoxybenzyloxy)nona-2,4-dienoate 
• 177977-21-8 (2E,4E)-9-(4-Methoxy-benzyloxy)-nona-2,4-dien-1-ol 

Downstream Products

• 383863-71-6 (1S,3aS,4R,5R,5aR,8aR,8bS)-4-Allyl-7-methoxy-5-[4-(4-methoxy-benzyloxy)-butyl]-1-methyl-2-oxo-decahydro-furo[3,2-e]indole-6-carboxylic acid methyl ester 
• 16625-37-9 stenine 

Relevant academic research and scientific papers

Stereocontrolled total synthesis of the Stemona alkaloid (-)-stenine

The Stemona alkaloid stenine (1), isolated from Stemona tuberosa of physiologically active stemonaceous plants, possesses the structurally novel and unique azepinoindole skeleton (B,C,D-ring system). We have achieved the asymmetric total synthesis of (-)-

Untersuchungen zur asymmetrischen Synthese von Stemona-Alkaloiden: Totalsynthese von (-)-Stenin

Keywords: Alkaloide; Asymmetrische Synthesen; (-)-Stenin; Totalsynthesen