210633-90-2

Upstream product

• 210633-87-7 C₂₀H₂₄O₆ 
• 210633-86-6 (3aR,4S,7R,7aS,8S,9R)-tetrahydro-8,9-dihydroxy-2,2,4-trimethyl-4,7-ethano-1,3-benzodioxol-5(4H)-one 
• 210633-85-5 (3aS,4R,7S,7aR)-3a,4,7,7a-tetrahydro-2,2,7-trimethyl-4,7-ethano-1,3-benzodioxol-8-one 
• 685108-94-5 (3aS,4R,4aS,6S,7aR,8S,8aR)-hexahydro-6-(4-methoxyphenyl)-2,2,8-trimethyl-4,8-ethanobenzo[1,2-d:4,5-d']bis[1,3]-dioxol-9-one 
• 685108-95-6 (3aR,4S,4aR,6S,7aS,8R,8aS)-hexahydro-6-(4-methoxyphenyl)-2,2,4-trimethyl-10-methylene-4,8-ethanobenzo[1,2-d:4,5-d']bis[1,3]dioxole 
• 210633-88-8 C₂₁H₂₆O₅ 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 

Downstream Products

• 210633-94-6 (3aR,4R,5S,6S,7S,7aS)-5-ethenylhexahydro-2,2,4-trimethyl-9-methylene-6-(phenylmethoxy)-4,7-ethano-1,3-benzodioxol-5-ol 

Relevant academic research and scientific papers

Taxane diterpene synthesis studies. Part 1: Chemoenzymatic and enantiodivergent routes to AB-ring substructures of taxoids and ent-taxoids

The microbially derived cis-1,2-dihydrocatechol 2 has been converted, via reaction sequences including Diels-Alder cycloaddition and anionic oxy-Cope rearrangement steps, into enantiopure bicyclo[5.3.1]undecenes 21 and 34, which correspond to AB-ring subs

From toluene to taxol: Chemoenzymatic and enantiodivergent routes to the AB-ring systems of taxoids and ent-taxoids

The cis-1,2-dihydrocatechol 2 has been converted, via reaction sequences including Diels-Alder cycloaddition and anionic oxy-Cope rearrangement steps, into the enantiopure bicyclo[5.3.1]undecanes 20 and 33 which correspond to the AB-ring systems of ent-ta