145741-52-2

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 145741-67-9 (+)-(1S,2S,3R,4R)-Ethyl 5-benzyloxy-3-tert-butyldimethylsilyloxy-4-ethoxycarbonylmethylcyclopentan-1-ol 
• 145741-66-8 (-)-(2E)-(4R,5S,6R)-5-Benzyloxy-4-tert-butyldimethylsilyloxy-7-(1',3'-dithiolan-2'-yl)-6-hydroxyhept-2-enoate 
• 108788-48-3 (Z)-3-((3aR,5R,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-acrylic acid ethyl ester 
• 145741-65-7 (-)-(2E)-(4R,5R,6R)-5-Benzyloxy-4,6-dihydroxy-7-(1',3'-dithiolan-2'-yl)hept-2-enoate 

Downstream Products

• 145741-53-3 (+)-(1S,2S,3R,4S)-2-Benzyloxy-4-(2'-hydroxyethyl)cyclopentane-1,3-diol 

Relevant academic research and scientific papers

Radical Cyclisation Reactions Leading to Polyhydroxylated Cyclopentane Derivatives: Synthesis of (1R,2R,3S,4R)- and (1S,2S,3R,4S)-4-Hydroxyethylcyclopentane-1,2,3-triol

The tetrol (-)-1 has been prepared from a derivative of (D)-allose 3.The stereoselective carbocyclization reaction (8->11) formed the key step in this sequence.The enantiomeric cyclopentane derivative (+)-1 was also prepared from compound 3.In this synthe