Synthesis and absolute configuration assignment of albucidin: a late-stage reductive deiodination by visible light photocatalysis

The synthesis of albucidin and its enantiomer are described. It involves a visible-light photocatalysis deiodination at the late stage. The absolute configuration of natural albucidin is determined as (1R, 3S). This work provides a basis for structural modification to develop a new type of herbicidal from an old structure.