Christopher R. Maxwell

Enantioselective Alkylative Double Ring Opening of Epoxides: Synthesis of Enantioenriched Unsaturated Diols and Amino Alcohols

David M. Hodgson, Christopher R. Maxwell, Timothy J. Miles et al. · Angewandte Chemie International Edition · 2002 · 41 citations

Engineering, Alkene Metathesis, External Chiral Ligands +12

6-Substituted 2-azabicyclo[2.2.1]hept-5-enes by nitrogen-directed radical rearrangement: synthesis of an epibatidine analogue with high binding affinity at the nicotinic acetylcholine receptorElectronic supplementary information (ESI) available: details of biological studies. See http://www.rsc.org/suppdata/p1/b1/b107414h/

David M. Hodgson, Christopher R. Maxwell, Richard Wisedale et al. · Journal of the Chemical Society Perkin Transactions 1 · 2001 · 27 citations

Bioorganic Chemistry, Peptide Science, Base-induced Isomerisation +16

Asymmetric rearrangement of N-Boc 7-azanorbornene oxide: use of aryllithiums for enantioselective deprotonation

David M. Hodgson, Christopher R. Maxwell, Ian R. Matthews · Tetrahedron Asymmetry · 1999 · 27 citations

N-boc 7-Azanorbornene Oxide, Chemical Engineering, Cross-coupling Reaction +9

An Epoxide Rearrangement - Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue

David M. Hodgson, Christopher R. Maxwell, Ian R. Matthews · Synlett · 1998 · 23 citations

Natural Product Synthesis, Radical Rearrangement Approach, Epoxide Rearrangement +13

Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols

David M. Hodgson, Christopher R. Maxwell, Timothy J. Miles et al. · Tetrahedron · 2004 · 21 citations

Unsaturated Amino Alcohols, Engineering, Organic Chemistry +5