383863-69-2

Upstream product

• 111-29-5 1 ,5-pentanediol 
• 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 
• 177977-00-3 1-((5E,7E)-9-Chloro-nona-5,7-dienyloxymethyl)-4-methoxy-benzene 
• 824-94-2 p-methoxybenzyl chloride 
• 131375-69-4 5-((4-methoxybenzyl)oxy)pentanal 
• 131375-63-8 5-(4-methoxybenzyloxy)-1-pentanol 
• 383863-67-0 {(1R,2R,4aS,8aR)-2-[4-(4-Methoxy-benzyloxy)-butyl]-6-oxo-7-trimethylsilanyloxy-1,2,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl}-carbamic acid methyl ester 
• 1052228-23-5 (3aR,4S,7R,7aR)-4-Carboxymethyl-2-hydroxy-7-[4-(4-methoxy-benzyloxy)-butyl]-2,3,3a,4,7,7a-hexahydro-indole-1-carboxylic acid methyl ester 
• 177977-13-8 (1R,2R,4aS,8aR)-2-[4-(4-Methoxy-benzyloxy)-butyl]-6-oxo-1,2,4a,5,6,7,8,8a-octahydro-naphthalene-1-carbothioic acid S-ethyl ester 

Downstream Products

• 16625-37-9 stenine 
• 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 
• 383863-70-5 (3aS,4R,5R,5aR,8aR,8bR)-4-Allyl-7-methoxy-5-[4-(4-methoxy-benzyloxy)-butyl]-2-oxo-decahydro-furo[3,2-e]indole-6-carboxylic acid methyl ester 

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