作者:Debra J. Wallace、Carl A. Baxter、Karel J. M. Brands、Nadine Bremeyer、Sarah E. Brewer、Richard Desmond、Khateeta M. Emerson、Jennifer Foley、Paul Fernandez、Weifeng Hu、Stephen P. Keen、Peter Mullens、Daniel Muzzio、Peter Sajonz、Lushi Tan、Robert D. Wilson、George Zhou、Guoyue Zhou
DOI:10.1021/op2000783
日期:2011.7.15
Compound (1) a poly(ADP-ribose)polymerase (PARP) inhibitor has been made by a fit-for-purpose large-scale synthesis using either a classical resolution or chiral chromatographic separation. The development and relative merits of each route are discussed, along with operational improvements and extensive safety evaluations of potentially hazardous reactions.