Equivalence of dimensional reduction and dimensional regularisation

For some years there has been uncertainty over whether regularisation by dimensional reduction (DRED) is viable for non-supersymmetric theories. We resolve this issue by showing that DRED is entirely equivalent to standard dimensional regularisation (DREG), to all orders in perturbation theory and for a general renormalisable theory. The two regularisation schemes are related by an analytic redefinition of the couplings, under which the -functions calculated using DRED transform into those computed in DREG. TheS-matrix calculated using DRED is numerically equal to the DREG version, ensuring that both schemes give the same physics.     

Design and Asymmetric Synthesis of beta-Strand Peptidomimetics

We describe the asymmetric synthesis of non-peptidic compounds that feature rigid backbone conformations and present various side-chain functions. The key step in the synthesis of these compounds is the C-acylation of an appropriate ketone with a suitably protected aspartic acid derivative. The resulting dipeptide modules may be connected to form tetrapeptide mimics. Specifically is described the mimicry of a four-residue segment of CD4, the cellular receptor of HIV-1. The design was based on molecular modeling and the X-ray crystal structures of CD4 and intended to present the most important side chains and backbone elements of the Phe43-Lys46 segment.