1440870-07-4

Upstream product

• 935550-27-9 ((1S,2S,4aR,8aS)-2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)methanol 
• 1440869-22-6 (10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-(2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)methanone 
• 1440869-16-8 1-(10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-dodeca-2,8,10-trien-1-one 
• 55489-11-7 6,6-dimethoxyhexanal 
• 1440870-02-9 (1R,6R,7aS)-allyl-7a-(3-((3,4-dimethoxybenzyl)oxy)propoxy)-6-((1S,2S,4aR,8aS)-2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-1-carbonyl)-5-oxo-6-(phenylthio)hexahydro-1H-pyrrolizine-1-carboxylate 
• 1440869-97-5 (2R,7S,7aS)-7-(((tert-butyldimethylsilyl)oxy)methyl)-7a-(3-((3,4-dimethoxybenzyl)oxy)propoxy)-2-((1S,2S,4aR,8aS)-2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-1-carbonyl)-2-(phenylthio)tetrahydro-1H-pyrrolizin-3(2H)-one 
• 95019-19-5 (6E,8E)-6,8-decadienal and (6Z,8E)-6,8-decadienal 
• 1440870-65-4 (7S,7aS)-7-(((tert-butyldimethylsilyl)oxy)methyl)-7a-(3-((3,4-dimethoxybenzyl)oxy)propoxy)-2-((1S,2S,4aR,8aS)-2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalene-1-carbonyl)tetrahydro-1Hpyrrolizin-3(2H)-one 
• 1440869-92-0 (7S,7aS)-7-(tert-butyldimethylsilyloxymethyl)-7a-[3-(3,4-dimethoxybenzyloxy)propoxy]-tetrahydro-1H-pyrrolizin-3(2H)-one 
• 1440870-60-9 (7S,7aS)-7a-[3-(3,4-dimethoxybenzyloxy)propoxy]-7-(hydroxymethyl)tetrahydro-1H-pyrrolizin-3(2H)-one 
• 1440869-82-8 [(1S)-7a-hydroxy-5-oxohexahydro-1H-pyrrolizin-1-yl]methyl benzoate 
• 1440869-73-7 (7S)-7-[(tert-butyldiphenylsilyloxy)methyl]-7a-hydroxytetrahydro-1H-pyrrolizin-3(2H)-one 
• 1440869-68-0 (5R,6S)-6-[(tert-butyldiphenylsilyloxy)methyl]-5-hydroxyazocan-2-one 
• 1440870-55-2 (5R,6S)-5-hydroxy-6-(hydroxymethyl)azocan-2-one 

Relevant academic research and scientific papers

Stereocontrolled total synthesis of (+)-UCS1025A

Under control: A stereocontrolled total synthesis of (+)-UCS1025A, a potent telomerase inhibitor, was achieved. The synthesis features an intramolecular Diels-Alder reaction, a tandem Staudinger/aza-Wittig reaction, and stereoselective construction of the hemiaminal moiety facilitated by neighboring-group participation. Copyright