Sultones and Sultines via a Julia-Kocienski Reaction of Epoxides

We thank the EPSRC/Syngenta for a CASE Ph.D. Studentship (to G.M.T.S. under grant EP/J50029X/1), the EPSRC UK National Mass Spectrometry Facility at Swansea University and the EPSRC UK National Crystallography Service Facility at Southampton University.37 We are indebted to Andrew Plant and Janice Black (Syngenta) for the initial suggestion of using the combination of LiN(SiMe3)2/CH2Cl2 and Matthew Reid (Syngenta) for NMR assistance

High regioselectivity in electrochemical α-methoxylation of N-protected cyclic amines

N-Protecting groups of α-substituted cyclic amines strongly affected the regioselectivity in electrochemical methoxylation of these compounds. Namely, N-acyl derivatives were transformed into α′-methoxylated compounds, while N-cyano derivatives changed into α-methoxylated derivatives. Furthermore, Lewis acid catalyzed nucleophilic substitution of the α-methoxylated compounds protected with cyano group afforded α,α-disubstituted cyclic amines

The barrier to enantiomerization and dynamic resolution of N-Boc-2-lithiopiperidine and the effect of TMEDA

The kinetics of enantiomerization and dynamic thermodynamic resolution (DTR) of N-Boc-2-lithiopiperidine have been measured, revealing significant differences in enthalpy and entropy for these processes and a role for the achiral ligand TMEDA: the racemization and the DTR are catalytic and first order in [TMEDA], and this has implications for asymmetric synthesis with chiral organolithiums