815577-90-3

Upstream product

• 75-11-6 diiodomethane 
• 815578-01-9 (1S,6S)-6-(benzyloxy)-2-iodo-1-methylcyclohex-2-enecarbaldehyde 
• 815577-89-0 (2R,4aR,8aS)-4a,7,8,8a-tetrahydro-5-iodo-4a-methyl-1-phenyl-4H-benzo[d][1,3]dioxine 
• 815578-00-8 ((1R,6S)-6-(benzyloxy)-2-iodo-1-methylcyclohex-2-enyl)methanol 
• 815577-88-9 (2R,4aR,8aS)-hexahydro-4a-methyl-2-phenylbenzo[d][1,3]dioxin-5-one 
• 619335-62-5 (2R,3S)-2-Benzyloxymethyl-3-hydroxy-2-methyl-cyclohexanone 
• 619335-75-0 (2R,3S)-3-hydroxy-2-hydroxymethyl-2-methylcyclohexanone 

Downstream Products

• 815577-91-4 1-(((S)-((5S,6S)-5-benzyloxy-6-methyl-6-vinylcyclohex-1-enyl)((S)-3-iodo-1-(methoxymethoxy)-2,2,4-trimethylcyclohex-3-enyl)methoxy)methyl)benzene 
• 954096-35-6 C₃₃H₄₁IO₃ 
• 815578-02-0 (S)-((5S,6S)-5-benzyloxy-6-methyl-6-vinylcyclohex-1-enyl)((S)-3-iodo-1-(methoxymethoxy)-2,2,4-trimethylcyclohex-3-enyl)methanol 

Relevant academic research and scientific papers

Synthetic studies on the taxane skeleton: Construction of eight-membered carbocyclic rings by the intramolecular B-alkyl Suzuki-Miyaura cross-coupling reaction

(Chemical equation presented) Construction of eight-membered carbocyclic rings via the intramolecular B-alkyl Suzuki-Miyaura cross-coupling reaction has been studied. This protocol proved its potency through the formation of the eight-membered ring posses