198954-23-3Relevant academic research and scientific papers
Enantioselective introduction of a benzenesulfonylmethyl substituent at an unactivated carbon atom via chemoenzymatic methods
Maguire, Anita R.,Kelleher, Leonard L.
, p. 7459 - 7462 (2007/10/03)
Introduction of a benzenesulfonylmethyl group at the unactivated γ-carbon of carboxylic acid derivatives has been achieved through a combination of rhodium acetate catalysed carbenoid C-H insertion and baker's yeast mediated kinetic resolution. Access to
