77003-57-7

Upstream product

• 98-88-4 benzoyl chloride 
• 77003-54-4 (3R,4R,5R)-3-benzoyloxy-4,5-dihydroxycyclohexanone 4,5-O-cyclohexylidene acetal 
• 77003-55-5 (7R,8R,9R)-9-benzoyloxy-7,8-dihydroxy-1,4-dithiaspiro<4.5>decane 
• 77003-56-6 (2R)-2-benzoyloxy-4-oxo-1,6-hexanedial 4-ethylene dithioacetal 

Downstream Products

• 83182-00-7 (2R)-1-benzoyloxy-5-(5,5-dimethyl-1,3-dioxan-2-yl)-2-methanesulphonyloxypentan-4-one ethylene dithioacetal 
• 83181-96-8 (2R)-1-benzoyloxy-2-methanesulfonyloxy-6-(t-butyldimethylsiloxy)hexan-4-one ethylene dithioacetal 
• 83181-99-1 (2R)-1-benzoyloxy-5-formyl-2-methylsulphonyloxypentan-4-one ethylene dithioacetal 
• 83181-95-7 (2R)-1-benzoyloxy-2-hydroxy-6-(t-butyldimethylsilyloxy)-hexan-4-one ethylene dithioacetal 
• 83181-97-9 (2R)-1-benzoyloxy-6-hydroxy-2-methanesulfonyloxyhexan-4-one ethylene dithioacetal 
• 77003-63-5 (2R)-1-benzoyloxy-2-carbamoyloxy-7,9-dioxadecan-4-one ethylene dithioacetal 
• 77003-60-2 (2R)-1-benzoyloxy-2-hydroxy-7,9-dioxadecan-4-one ethylene dithioacetal 
• 77003-58-8 (2R)-1-benzoyloxy-2,6-dihydroxyhexan-4-one ethylene dithioacetal 

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

Studies Related to Maytansinoids

(3R, 4R, 5R)-3-Benzoyloxy-4,5-dihydroxycyclohexanone ethylene dithioacetal (10), a compound elaborated from D-(-)-quinic acid, was cleaved at the cis-diol position by the use of triphenylbismuth carbonate.The resulting dialdehyde (11) was converted, in se