Journal of the American Chemical Society, Vol.117, No.13, 3705-3716, 1995
Sequenced Reactions with Samarium(II) Iodide - Tandem Intramolecular Nucleophilic Acyl Substitution/Intramolecular Barbier Cyclizations
Samarium(II) iodide has been employed to promote a tandem intramolecular nucleophilic acyl substitution/intramolecular Barbier cyclization sequence, generating bicyclic and tricyclic ring systems in excellent yield and high diastereoselectivity. Additionally, a highly versatile ring expansion-cyclization sequence allows entry into several different naturally occurring tricyclic ring systems containing seven- and eight-membered rings.
Keywords:CATION-STABILIZING AUXILIARY;CARBONYL ADDITION-REACTIONS;HIGHLY EFFECTIVE SYSTEM;RADICAL CYCLIZATION;ORGANIC-SYNTHESIS;POLYCYCLE CONSTRUCTION;ASYMMETRIC INDUCTION;COPE REARRANGEMENT;HALOGEN EXCHANGE;STRATEGY