88733-70-4

Upstream product

• 108-86-1 bromobenzene 
• 91988-36-2 C₂₁H₂₆O₅ 
• 89002-26-6 10,10-ethylenedioxy-3β-benzyloxy-8,9-dihydroxy-4,4-dimethyl-1α,2β,6β,7α-tricyclo<5.2.1.0^2.6>decane 
• 89002-25-5 10,10-ethylenedioxy-3β-benzyloxy-4,4-dimethyl-1α,2β,6β,7α-tricyclo-<5.2.1.0^2.6>dec-8-ene 
• 82431-54-7 C₁₄H₂₀O₃ 
• 89002-31-3 C₂₇H₃₇F₃O₈S 
• 89002-32-4 C₂₆H₃₇IO₅ 
• 89002-28-8 3,3-(ethylenedioxy)-2β-(trimethylacetoxymethyl)-4β-(hydroxymethyl)-6α-benzyloxy-7,7-dimethyl-1α,5α-bicyclo<3.3.0>octane 
• 89002-33-5 3,3-(ethylenedioxy)-2β-(trimethylacetoxymethyl)-6α-benzyloxy-4β,7,7-trimethyl-1α,5α-bicyclo<3.3.0>octane 
• 89002-27-7 3,3-(ethylenedioxy)-2β,4β-bis-(hydroxymethyl)-6α-benzyloxy-7,7-dimethyl-1α,5α-bicyclo<3.3.0>octane 
• 88733-65-7 3,3-(ethylenedioxy)-2β-hydroxymethyl-6α-benzyloxy-4β,7,7-trimethyl-1α,5α-bicyclo<3.3.0>octane 
• 88733-65-7 C₂₁H₃₀O₄ 

Downstream Products

• 91988-51-1 3,3-(ethylenedioxy)-6α-benzoyloxy-2β-carbomethoxy-4β,7,7-trimethyl-1α,5α-bicyclo<3.3.0>octane 
• 82881-09-2 6α-benzoyloxy-4α,7,7-trimethyl-1α,5α-bicyclo<3.3.0>octan-3-one 
• 82881-09-2 6α-benzoyloxy-4β,7,7-trimethyl-1α,5α-bicyclo<3.3.0>octan-3-one 
• 91988-47-5 C₂₂H₂₈O₆ 

Relevant academic research and scientific papers

THE SYNTHESIS OF dl-CORIOLIN

The synthesis of dienone 2, which has previously been converted into the title compound in one step, is described.The methanoindene 7 is transformed into dienone-alcohol 58 in eighteen steps (12percent overall yield).This was then hydroxylated at C-8, usi

THE SYNTHESIS OF d,l-CORIOLIN

The formal synthesis of coriolin (1) from methanoindene 2 is described.

A FACILE METHOD FOR THE OXIDATIVE REMOVAL OF BENZYL ETHERS: THE OXIDATION OF BENZYL ETHERS TO BENZOATES BY RUTHENIUM TETRAOXIDE

A series of benzyl ethers has been prepared and their oxidation to benzoate esters by ruthenium tetraoxide has been studied.Yields for the oxidation step range from 54 to 96 percent.