Woodward Informatics Ltd

Selected Academic Peer Reviewed Publications

Chiral glycine cation equivalents: N-acyliminium species derived from diketopiperazines. , Bull, S. D.; Davies, S. G.; Garner, A. C.; O'Shea, M. D.; Savory, E. D.; Snow, E. J. J. Chem. Soc., Perkin Trans. 1. 2002, (22), 2442. PDF(254kb)

Conjugate additions of organocuprates to a 3-methylene-6-isopropyldiketopiperazine acceptor for the asymmetric synthesis of homochiral β-amino acids. , Bull, S. D.; Davies, S. G.; Garner, A. C.; O'Shea, M. D. J. Chem. Soc., Perkin Trans. 1. 2001, (24), 3281. PDF(139kb)

Stereoselective conjugate addition of organocuprates to a dehydroalanine derived diketopiperazine. , Bull, S. D.; Davies, S. G.; O'Shea, M. D. J. Chem. Soc., Perkin Trans. 1. 1998, (22), 3657. PDF(141kb)

Synthetic approaches to the Angucyclinone antibiotics: A concise entry to the ring system of PD 116740 and TAN 1085. , Larsen, D. S.; O'Shea, M. D. J. Org. Chem. 1996, (61), 5681. PDF(200kb) and, for supporting information, PDF(329kb)

Total syntheses of the Angucyclinone antibiotics (+) Emycin A and (+) Ochromycinone. , Brooker, S.; Larsen, D. S.; O'Shea, M. D. Chem Commun. 1996, 203. PDF(276kb)

Synthetic approaches to the Angucyclinone antibiotics: The total synthesis of (±) Rubiginone B1 and B2, (±) Emycin A, and related analogues. , Larsen, D. S.; O'Shea, M. D. J. Chem. Soc., Perkin Trans. 1. 1995, 1019. PDF(1540kb)

A stereoselective approach to the Angucyclinone antibiotics: A total synthesis of (±) Rubiginone B1. , Larsen, D. S.; O'Shea, M. D. Tetrahedron Lett. 1993, (34), 3679.

A stereoselective approach to the Angucyclinone antibiotics: A total synthesis of the C-1 epimer of (±) Rubiginone B1. , Larsen, D. S.; O'Shea, M. D. Tetrahedron Lett. 1993, (34), 1373.

International Conference Presentations

A Software System for Automated HTA in Heterogeneous Empower, ChemStation, and MassLynx Controlled Analytical Systems Using a Single Common User Interface. , see Consult-igma or Tessella for the Chromatographic Society abstract for this lecture.