1354635-38-3

Upstream product

• 1354635-37-2 (1S,2S)-2-formyl-2,3-dihydro-2,6-dimethyl-1H-inden-1-yl4-nitrobenzoate 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 1354635-35-0 (1S,2R)-2,3-dihydro-2-(hydroxymethyl)-2,6-dimethyl-1H-inden-1-yl 4-nitrobenzoate 
• 1354635-33-8 (1S,2R)-2-((tert-butyldimethylsilyloxy)methyl)-2,3-dihydro-2,6-dimethyl-1H-inden-1-yl 4-nitrobenzoate 
• 1354635-31-6 (1S,2R)-2-((tert-butyldimethylsilyloxy)methyl)-2,3-dihydro-2,6-dimethyl-1H-inden-1-ol 
• 1354634-98-2 (1S,2R)-2,3-dihydro-2-(hydroxymethyl)-2,6-dimethyl-1H-inden-1-ol 
• 1073511-11-1 (R)-2,3-dihydro-2-(hydroxymethyl)-2,6-dimethylindane-1-one 
• 285977-95-9 2-(hydroxymethyl)-2,6-dimethyl-2,3-dihydro-1H-inden-1-one 

Relevant academic research and scientific papers

Enantiomeric scaffolding of α-tetralone and related scaffolds by EKR (Enzymatic Kinetic Resolution) and stereoselective ketoreduction with ketoreductases

Stereochemically pure compounds containing an all carbon quaternary stereocenter based on 1-tetralone, 1-indanone and 4-chromanone scaffolds have been synthesized by employing Lipase PS (Burkholderia cepacia) catalyzed kinetic resolution. These scaffolds