Aminative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: a novel stereocontrolled route to substituted pyrrolidinesElectronic supplementary information (ESI) available: experimental details and characterisation data for all new compounds. See http://www.rsc.org/suppdata/cc/b3/b316554j/
Armstrong, Alan; Cumming, Graham R.; Pike, Kurt; Armstrong Alan; Department of Chemistry, Imperial College London; Cumming Graham R.; Department of Chemistry, Imperial College London; Pike Kurt; CVGI Chemistry, AstraZeneca
Журнал:
Chemical Communications
Дата:
2004
Аннотация:
Aziridination of 2-alkoxy-3,4-dihydro-2H-pyrans leads to rearrangement and stereocontrolled formation of 5-alkoxypyrrolidines which may be reduced to pyrrolidines or allylated stereoselectively.
101.4Кб