142133-51-5

Upstream product

• 142186-74-1 (4aR,6R,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one 
• 142186-68-3 (1R,2R,3S,8S,10R,11S,13R)-10-(benzyloxy)-15,15-dimethyl-12,14,16-trioxatetracyclo<11.3.0.0^2,11.0^3,8>hexadecane-4,6-dione 
• 142186-73-0 (4aS,6R,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-1-methoxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-3-one 
• 142186-75-2 (4aR,6R,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-decahydro-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one 

Downstream Products

• 142186-76-3 Acetic acid (3aR,4aS,5R,7R,8S,8aR,8bR)-7-(4-acetoxy-butyl)-5-benzyloxy-2,2-dimethyl-octahydro-benzo[4,5]furo[2,3-d][1,3]dioxol-8-yl ester 

Relevant academic research and scientific papers

Tandem Intramolecular Michael Addition/Aldol Condensation or Acylation Applied to D-Glucose-Derived Substrates: Preparation of Enantiomeric Octahydronaphthalenone Derivatives Equipped with C- and O-Functionalities

An enantiomerically pure (1,2-isopropylidenedioxy)tetrahydrofuran derivative, 9, bearing acetonyl and propionaldehyde side chains smoothly underwent aldol cyclization under basic conditions.The major product was the cis-aldol 21S, accompanied by the trans