915122-91-7

Upstream product

• 5375-00-8 3-benzyloxypropyl iodide 
• 101693-93-0 (5R)-5-methyl-2-(phenylthio)cyclohexan-1-one 
• 54307-74-3 (R)-5-methyl-cyclohex-2-enone 
• 915122-88-2 [(3S,5R)-2-(3-Benzyloxy-propyl)-3-(3-iodo-prop-2-ynyl)-5-methyl-cyclohex-1-enyloxy]-tert-butyl-dimethyl-silane 
• 915122-93-9 [(3S,5R)-2-(3-Benzyloxy-propyl)-5-methyl-3-prop-2-ynyl-cyclohex-1-enyloxy]-tert-butyl-dimethyl-silane 
• 915122-89-3 (3aR,6R,7aS)-3a-(3-Benzyloxy-propyl)-3-iodo-6-methyl-1,3a,5,6,7,7a-hexahydro-inden-4-one 
• 915122-87-1 (R)-2-(3-Benzyloxy-propyl)-5-methyl-cyclohex-2-enone 
• 915122-92-8 (R)-5-methyl-2-iodo-2-cyclohexen-1-one 
• 915122-90-6 (3aS,6R,7aS)-3a-(3-Benzyloxy-propyl)-3-[(E)-3-(dimethyl-hydrazono)-propenyl]-6-methyl-1,3a,5,6,7,7a-hexahydro-inden-4-one 

Relevant academic research and scientific papers

A divergent and concise total synthesis of (-)-lycoposerramine R and (+)-lycopladine A

A concise, asymmetric and divergent synthesis of lycoposerramine R and lycopladine A is presented. The synthesis features the palladium-catalyzed cycloalkenylation of a silyl enol ether for assembling the 5/6-hydrindane system and generating a quaternary

Gold(I)-catalyzed cyclizations of silyl enol ethers: Application to the synthesis of (+)-lycopladine A

(Chemical Equation Presented) In control: Gold(I)-catalyzed intramolecular addition of silyl enol ethers to alkynes and allenes allows for the diastereoselective synthesis of cyclopentenes with control of the position of the double bond. The utility of th