155813-64-2

Upstream product

• 153185-64-9 Ethyl (4R)-4-<(4R)-2,2-diethyl-1,3-dioxolan-4-yl>-2-methyl-2-pentenoate 
• 155813-59-5 Ethyl (2S)-2-<(2S,3R,4R)-4-acetoxy-3-methyltetrahydrofuran-2-yl>propionate 
• 183947-36-6 (S)-2-((R)-2,2-Diethyl-[1,3]dioxolan-4-yl)-propionaldehyde 
• 153185-63-8 (2R,3R)-3,4-diethylmethylenedioxy-2-methyl-butan-1-ol 
• 155813-57-3 (S)-2-((2S,3S,4R)-4-Hydroxy-3-methyl-tetrahydro-furan-2-yl)-2-iodo-propionic acid ethyl ester 
• 74213-61-9 diethyl (2S,3R)-3-hydroxy-2-methylsuccinate 
• 74213-65-3 (2R,3R)-3-methyl-butan-1,2,4-triol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 155813-60-8 (3R,4S,5R)-5-((R)-2-Hydroxy-1-methyl-ethyl)-4-methyl-tetrahydro-furan-3-ol 
• 155813-58-4 Ethyl (2S)-2-<(2S,3R,4R)-4-acetoxy-3-methyltetrahydrofuran-2-yl>-2-iodopropionate 

Downstream Products

• 155813-65-3 (2R)-1-<(tert-Butyldiphenylsilyl)oxy>-2-<(2R,3R,4R)-4-methoxy-3-methyltetrahydrofuran-2-yl>propane 

Relevant academic research and scientific papers

Stereoselective Hydrogen Transfer Reactions Involving Acyclic Radicals. Tandem Substituted Tetrahydrofuran Formation and Stereoselective Reduction: Synthesis of the C17-C22 Subunit of Ionomycin

The tandem iodoetherification reaction and stereoselective reduction of acyclic redicals has been used in the stereocontrolled synthesis of substituted tetrahydrofurans.Such a tetrahydrofuran intermediate is regioselectively cleaved using Me2BBr to reveal