153977-33-4

Upstream product

• 110653-58-2 (2R,3R,4S)-4-benzyloxymethyl-3-formyloxy-2-methylhexanal 
• 152934-36-6 (2S,3S,4S)-4-Benzyloxymethyl-3-hydroxy-2-methyl-1-pivaloyloxyhexane 
• 152934-35-5 (2S,3S,4S)-4-Benzyloxymethyl-2-methylhexane-1,3-diol 
• 152934-37-7 (2S,3S,4S)-2-Ethyl-4-methyl-5-pivaloyloxypentane-1,3-diol 
• 156479-44-6 (3R,4S,5S)-4-acetoxy-6-benzyloxymethoxy-5-methyl-3-(4-methylphenylsulfonyloxymethyl)hex-1-ene 
• 156479-43-5 (2S,3S,4R)-1-benzyloxymethoxy-2-methyl-4-(4-methylphenylsulfonyloxymethyl)hex-5-en-3-ol 
• 156479-45-7 (3S,4S,5S)-4-acetoxy-6-benzyloxymethoxy-3-ethyl-5-methylhex-1-ene 
• 156479-42-4 (2R,3S,4S)-5-benzyloxymethoxy-4-methyl-2-vinylpentane-1,3-diol 
• 156479-48-0 (2S,3S,4S)-1-benzyloxymethoxy-4-ethyl-3,5-isopropylidenedioxy-2-methylpentane 
• 156479-47-9 (2S,3S,4S)-5-benzyloxymethoxy-2-ethyl-4-methylpentane-1,3-diol 
• 156557-41-4 (4S)-5-benzyloxymethyloxy-2,3-epoxy-4-methylpentan-1-ol 
• 152934-39-9 (2S)-2-<(4S,5S)-5-Ethyl-2,2-dimethyl-1,2-dioxan-4-yl>propan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 152934-38-8 (4S,5S,1'S)-2,2-dimethyl-5-ethyl-4-<1'-methyl-2'-(trimethylacetoxy)ethyl>-1,3-dioxane 

Downstream Products

• 156479-49-1 (2S,3R,4R)-2-ethyl-1,3-isopropylidenedioxy-4-methyl-5-phenylthiopentane 
• 131927-95-2 (2S)-2-<(2S,3S,5S)-5-<(2R,5S)-5-((1R)-Benzyloxymethoxyethyl)-5-ethyltetrahydrofur-2-yl>-5-<(1E)-2-(4-methoxyphenyl)ethenyl>-3-methyltetrahydrofur-2-yl>butan-1-ol 
• 131927-95-2 (2S)-2-<(2S,3S,5R)-5-<(2R,5S)-5-((1R)-Benzyloxymethoxyethyl)-5-ethyltetrahydrofur-2-yl>-5-<(1E)-2-(4-methoxyphenyl)ethenyl>-3-methyltetrahydrofur-2-yl>butan-1-ol 
• 132016-49-0 (2S)-2-<(2S,3S,5S)-5-<(2R,5R,6S)-5-Benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-5-<(1E)-2-(4-methoxyphenyl)ethenyl>-3-methyltetrahydrofur-2-yl>butan-1-ol 
• 131927-94-1 (2S)-2-<(2S,3S,5R)-5-<(2R,5R,6S)-5-Benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-5-<(1E)-2-(4-methoxyphenyl)ethenyl>-3-methyltetrahydrofur-2-yl>butan-1-ol 
• 152934-55-9 Benzyl 23-O-benzyloxymethylisolasalocid A 
• 152934-45-7 (2S)-2-<(2S,3S,5R)-5-<(2R,5S)-5-((1R)-Benzyloxymethoxyethyl)-5-ethyltetrahydrofur-2-yl>-5-<(1E)-2-(4-methoxyphenyl)ethenyl>-3-methyltetrahydrofur-2-yl>butyl tert-butyldimethylsilyl ether 
• 152934-52-6 (2S)-2-<(2S,3S,5R)-5-<(2R,5R,6S)-5-Benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-5-<(1E)-2-(4-methoxyphenyl)ethenyl>-3-methyltetrahydrofur-2-yl>butyl tert-butyldimethylsilyl ether 
• 54156-67-1 Isolasalocid A 
• 152934-54-8 (2S)-2-<(2S,3S,5S)-5-<(2R,5R,6S)-5-Benzyloxy-5-ethyl-6-methyltetrahydropyran-2-yl>-5-formyl-3-methyltetrahydrofur-2-yl>butyl tert-butyldimethylsilyl ether 
• 152934-48-0 {(S)-2-[(2R,4S,5S,2'R,5'S)-5'-((R)-1-Benzyloxymethoxy-ethyl)-5'-ethyl-4-methyl-2-vinyl-octahydro-[2,2']bifuranyl-5-yl]-butoxy}-tert-butyl-dimethyl-silane 

Relevant academic research and scientific papers

Stereoselective Total Synthesis of Polyether Ionophore Antibiotics, Isolasalocid A and Lasalocid A. Part 2. The Total Synthesis via Stereoselective Construction of the B Rings by Chelation-Controlled Cyclization under Thermodynamic Conditions

Stereoselective total synthesis of isolasalocid A (1) and lasalocid A (2) was achieved via construction of the tetrahydrofuran rings by chelation-controlled cyclization of the corresponding p-methoxyphenyl substituted allyl alcohols (6, 7) under thermodyn

Stereoselective synthesis of optically active 4-ethyl-3,5-dihydroxy-2- methylpentyl derivatives. A basic building block with three contiguous chiral centers of polyether antibiotics

Optically active 4-ethyl-3,5-dihydroxy-2-methylpentyl derivatives, the iodide (4), phenyl sulfone (5), and phenyl sulfoxide (6), which are chiral synthons for an essential structural unit of polyether antibiotics, were stereoselectively synthesized starti