Synthesis and biomimetic rearrangement of a chiral diterpene dioxide

As pan of a biomimetic approach towards me marine triterpene teurilene (2), the synthesis of the chiral diepoxide 3 is described. Aiming at the synthesis of the squalene tetraepoxide 1, double Sharpless epoxidation led to the intermediate bisglycidic alcohol 7 being subject to a stereochemical analysis.     

Groupwise density and the cofinality of the infinite symmetric group

We study the relationship between the cofinality of the infinite symmetric group and the cardinal invariants and . In particular, we prove the following two results. Theorem 0.1 It is consistent with ZFC that there exists a simple $P_{\omega_{1}}$ -point and that $c(Sym(\omega)) = \omega_{2} = 2^{\omega}$ . Theorem 0.2 If there exist both a simple $P_{\omega_{1}}$ -point and a $P_{\omega_{2}}$ -point, then $c(Sym(\omega)) = \omega_{1}$ . Received: 7 March 1996     

A convection/reaction/switching system

We consider a spatially distributed hybrid system consisting of a convection/reaction system in which the reaction switches discontinuously in time between modes, independently at each spatial point on reaching “switching thresholds”. The model involves a novel formulation for evolution of the free boundary between the modal regions.     

Novel Technique for All-Optical Clock Extraction Using Fiber Bragg Gratings

We demonstrate a simple passive technique, using phase shifted fibre Bragg gratings, for extraction of optical clock signals from RZ optical data signals . The generation of an optical clock signal at 12.5 GHz from a 12.5 Gbs RZ optical data stream is experimentally demonstrated with simulation of optical clock extraction at 10 GHz fro m 40 Gbs OTDM data streams .     

Cell transfer and monomial positivity

We give combinatorial proofs that certain families of differences of products of Schur functions are monomial-positive. We show in addition that such monomial-positivity is to be expected of a large class of generating functions with combinatorial definitions similar to Schur functions. These generating functions are defined on posets with labelled Hasse diagrams and include for example generating functions of Stanley's (P,ω)-partitions. T.L. was supported in part by NSF DMS-0600677.     

Dynamic supercoiling bifurcations of growing elastic filaments

Certain bacteria form filamentous colonies when the cells fail to separate after dividing. In Bacillus subtilis, Bacillus thermus, and Cyanobacteria, the filaments can wrap into complex supercoiled structures as the cells grow. The structures may be solenoids or plectonemes, with or without branches in the latter case. Any microscopic theory of these morphological instabilities must address the nature of pattern selection in the presence of growth, for growth renders the problem nonautonomous and the bifurcations dynamic. To gain insight into these phenomena, we formulate a general theory for growing elastic filaments with bending and twisting resistance in a viscous medium, and study an illustrative model problem: a growing filament with preferred twist, closed into a loop. Growth depletes the twist, inducing a twist strain. The closure of the loop prevents the filament from unwinding back to the preferred twist; instead, twist relaxation is accomplished by the formation of supercoils. Growth also produces viscous stresses on the filament which even in the absence of twist produce buckling instabilities. Our linear stability analysis and numerical studies reveal two dynamic regimes. For small intrinsic twist the instability is akin to Euler buckling, leading to solenoidal structures, while for large twist it is like the classic writhing of a twisted filament, producing plectonemic windings. This model may apply to situations in which supercoils form only, or more readily, when axial rotation of filaments is blocked. Applications to specific biological systems are proposed.