622785-65-3

Upstream product

• 222309-45-7 2,2-dimethyl-3a,9b-dihydro-naphtho[1,2-d][1,3]dioxole 
• 622785-64-2 (3aS,4R,5R,9bR)-3a,4,5,9b-tetrahydro-2,2-dimethylnaphtho[1,2-d]-1,3-dioxole-4,5-diol 

Downstream Products

• 473543-36-1 (4S-cis)-5-[2'-(formyl)phenyl]-2,2-dimethyl-1,3-dioxolane-4-methanol acetate 
• 473543-38-3 (1S)-1-((4S,5R)-2,2-dimethyl-5-phenyl-[1,3]-dioxolan-4-yl)-3-buten-1-ol 
• 473543-39-4 (1R)-1-((4S,5R)-2,2-dimethyl-5-phenyl-[1,3]-dioxolan-4-yl)-3-buten-1-ol 
• 473543-35-0 (4S-cis)-5-[2'-(formyl)phenyl]-2,2-dimethyl-1,3-dioxolane-4-methanol 
• 162600-00-2 ((4S,5R)-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-yl)methanol 
• 473543-37-2 (4S-cis)-5-phenyl-2,2-dimethyl-1,3-dioxolane-4-methanol acetate 
• 130718-77-3 (4R,5R)-cis-2,2-dimethyl-5-phenyl-1,3-dioxolan-4-carbaldehyde 
• 160707-67-5 (4S-cis)-5-[2'-(hydroxymethyl)phenyl]-2,2-dimethyl-1,3-dioxolane-4-methanol 

Relevant academic research and scientific papers

A total synthesis of the styryllactone (+)-goniodiol from naphthalene

The cytotoxic natural product (+)-goniodiol (1) has been prepared in twelve steps from the enantiomerically pure cis-dihydrocatechol (2), which is readily obtained by microbial oxidation of naphthalene. Elaboration of compound (2) involves an initial oxid

A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene

The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, has been converted, via a sequence of reactions including oxidative C-C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural p