82302-51-0

Upstream product

• 78907-87-6 (3R,4S,5R)-5-O-benzyl-3,4,5-trihydroxycyclohexanone ethylene dithioacetal 
• 78907-88-7 (2R)-2-benzyloxy-4-oxo-1,6-hexanedial 4-ethylene dithioacetal 

Downstream Products

• 82302-52-1 (3R)-3-benzyloxy-1-cyclopentene-1-carbaldehyde propylene acetal 

Relevant academic research and scientific papers

Synthesis of Enantiomerically Pure Substituted Cyclopentenes from (-)-Quinic Acid

The synthesis of a large variety of enantiomerically pure substituted reactive cyclopentenes 16, 23, 24 and 28 have been synthesized from the readily available (-)-quinic acid 1.The straightforward strategy involves a high-yielding intramolecular aldoliza

Hetero-prostaglandin derivatives and processes for preparing them

Prostanoic acid derivatives represented by the general formula: STR1 in which X represents hydrogen or hydroxy, X1 represents hydrogen or X and X1, when they are taken together with the carbon atom to which they are attached, represent a carbonyl group and Z represents hydrogen or hydroxy and pharmaceutically acceptable alkali metal salts thereof. They can be used as bronchodilators and/or inhibitors of blood-platelet aggregation.