142186-68-3

Upstream product

• 142133-21-9 (1R,3S,4R,5R)-3-<(1R,3E)-1-(benzyloxy)-4-(ethoxycarbonyl)-3-butenyl>-4-(2-oxopropyl)-7,7-dimethyl-2,6,8-trioxabicyclo<3.3.0>octane 

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 
• 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 
• 142133-51-5 C₂₂H₂₈O₆ 
• 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 
• 142133-50-4 (4aS,6R,6aS,7aR,10aR,10bR,10cR)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-3-one 

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