Enantio- and diastereodifferentiating cis,trans-photoisomerization of 2beta,3beta-diphenylcyclopropane-1alpha-carboxylic acid derivatives in organized media

[reaction: see text] Four methods of asymmetric induction in the cis, trans-photoisomerization of 2beta, 3beta-diphenylcyclopropane-1alpha-carboxylic acid derivatives were studied. Best results (ca. 80% de) were obtained by irradiation of chiral esters, amides, and salts in NaY and LiY zeolites and in the pure crystalline state.     

Synthesis of proline-modified analogues of the neuroprotective agent glycyl-l-prolyl-glutamic acid (GPE)

The synthesis of ten proline-modified analogues of the neuroprotective tripeptide GPE is described. Five of the analogues incorporate a proline residue with a hydrophobic group at C-2 and two further analogues have this side chain locked into a spirolactam ring system. The pyrrolidine ring was also modified by replacing the γ-CH₂ group with sulfur and/or incorporation of two methyl groups at C-5.     

On the Dimension of Posets with Cover Graphs of Treewidth 2

In 1977, Trotter and Moore proved that a poset has dimension at most 3 whenever its cover graph is a forest, or equivalently, has treewidth at most 1. On the other hand, a well-known construction of Kelly shows that there are posets of arbitrarily large dimension whose cover graphs have treewidth 3. In this paper we focus on the boundary case of treewidth 2. It was recently shown that the dimension is bounded if the cover graph is outerplanar (Felsner, Trotter, and Wiechert) or if it has pathwidth 2 (Biró, Keller, and Young). This can be interpreted as evidence that the dimension should be bounded more generally when the cover graph has treewidth 2. We show that it is indeed the case: Every such poset has dimension at most 1276.