1301703-41-2

Upstream product

• 1301703-43-4 (3aR,4R,5R,6R,7S,7aR)-dibenzyl 5,6-dihydroxy-2,2-dimethylhexahydro-4,7-(epoxyimino)benzo[d][1,3]dioxole-3a,8-dicarboxylate 
• 1301703-46-7 (3aS,4R,5R,6R,7S,7aR)-7-ammonio-4,5,6-trihydroxy-2,2-dimethylhexahydrobenzo[d][1,3]dioxole-3a-carboxylate 
• 1301703-27-4 (3aS,7aR)-benzyl 2,2-dimethyl-3a,7a-dihydrobenzo[d][1,3]dioxole-3a-carboxylate 
• 1301703-31-0 (3aR,4R,7S,7aR)-dibenzyl 2,2-dimethyl-3a,4,7,7a-tetrahydro-4,7-(epoxyimino)-benzo[d][1,3]dioxole-3a,8-dicarboxylate 
• 32359-20-9 (1S,2R)-1,2-dihydroxycyclohexa-3,5-diene-1-carboxylic acid 
• 172877-74-6 (-)-(3aS,7aR)-2,2-dimethyl-3a,7a-dihydrobenzo[d][1,3]dioxole-3a-carboxylic acid 

Relevant academic research and scientific papers

"Inosaminoacids": Novel inositol-amino acid hybrid structures accessed by microbial arene oxidation

Microbial 1,2-dihydroxylation of sodium benzoate permits the rapid construction of novel inositol-amino acid hybrid structures. Both β- and γ-amino acids are accessible by means of an acylnitroso Diels-Alder cycloaddition. The Royal Society of Chemistry 2