866650-91-1

Upstream product

• 866650-90-0 (1R,2S,5S)-2-(tert-Butyl-dimethyl-silanyloxymethyl)-8,8-dimethyl-6-oxa-bicyclo[3.2.1]octan-7-one 
• 866650-89-7 (1R,2S,5S)-2-Hydroxymethyl-8,8-dimethyl-6-oxa-bicyclo[3.2.1]octan-7-one 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 358339-06-7 (1R,5S)-(+)-8,8-dimethyl-2-methylene-6-oxabicyclo[3.2.1]octan-7-one 

Downstream Products

• 866650-92-2 [(1R,3S,6S)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-3-hydroxy-2,2-dimethyl-cyclohexyl]-hydroxy-acetonitrile 
• 866650-93-3 [(1R,6S)-6-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-cyclohexyl]-acetonitrile 
• 866650-97-7 (1S,2R)-2-(2-Furan-3-yl-2-oxo-ethyl)-3,3-dimethyl-cyclohexanecarboxylic acid 
• 866650-96-6 (1S,2R)-2-(2-Furan-3-yl-2-oxo-ethyl)-3,3-dimethyl-cyclohexanecarbaldehyde 

Relevant academic research and scientific papers

Enantioselective synthesis of (+)-ricciocarpin A using an auxiliary hydroxyl group and a diastereofacial selectivity based methodology

An enantioselective synthesis of (+)-ricciocarpin A is described starting from (+)-karahana lactone as an enantiopure building block. This synthesis involves a stereofacially directed diastereoselective hydroboration for the installation of the required s