Hamiltonian and long paths in bipartite graphs with connectivity

Let G be a graph, $\nu (G)$ the order of G, $\kappa (G)$ the connectivity of G and k a positive integer such that $k\le (\nu (G)?2)/2$. Then G is said to be k-extendable if it has a matching of size k and every matching of size k extends to a perfect matching of G. A Hamiltonian path of a graph G is a spanning path of G. A bipartite graph G with vertex sets $V_1$ and $V_2$ is defined to be Hamiltonian-laceable if such that $|V_1|=|V_2|$ and for every pair of vertices $p\in V_1$ and $q\in V_2$, there exists a Hamiltonian path in G with endpoints p and q, or $|V_1|=|V_2|+1$ and for every pair of vertices $p,q\in V_1,p\ne q$, there exists a Hamiltonian path in G with endpoints p and q. Let G be a bipartite graph with bipartition $(X,Y)$. Define $bn(G)$ to be a maximum integer such that $0\le bn(G)<min\{|X|,|Y|\}$ and (1) for each non-empty subset S of X, if $|S|\le |X|?bn(G)$, then $|N(S)|\ge |S|+bn(G)$, and if $|X|?bn(G)<|S|\le |X|$, then $N(S)=Y$; and (2) for each non-empty subset S of Y, if $|S|\le |Y|?bn(G)$, then $|N(S)|\ge |S|+bn(G)$, and if $|Y|?bn(G)<|S|\le |Y|$, then $N(S)=X$; and (3) $bn(G)=0$ if there is no non-negative integer satisfying (1) and (2).Let G be a bipartite graph with bipartition $(X,Y)$ such that $|X|=|Y|$ and $bn(G)>0$. In this paper, we show that if $\nu (G)\le 2\kappa (G)+4bn(G)?4$, then G is Hamiltonian-laceable; or if $\nu (G)>6bn(G)?2$, then for every pair of vertices $x\in X$ and $y\in Y$, there is an $(x,y)$-path P in G with $|V(P)|\ge 6bn(G)?2$. We show some of its corollaries in k-extendable, bipartite graphs and a conjecture in k-extendable graphs.     

Asymmetric Total Syntheses,Stereostructures, and Cytotoxicities of Marine Bromotriterpenoids Aplysiol B (Laurenmariannol) and Saiyacenol A

There are marine cytotoxic bromotriterpenoids, named the thyrsiferol family that are structurally characterized by some tetrahydropyran (THP) and tetrahydrofuran (THF) rings. The thyrsiferol family belongs to natural products that are often difficult to determine their stereostructures even by the current, highly advanced spectroscopic methods, especially in acyclic systems including stereogenic tetrasubstituted carbon centers. In such cases, it is effective to predict and synthesize the possible stereostructures. Herein, to elucidate ambiguous stereostructures and unassigned absolute configurations of aplysiol B, laurenmariannol, and saiyacenol A, members of the thyrsiferol family, we carried out their asymmetric chemical syntheses featuring 6-exo and 5-exo oxacyclizations of epoxy alcohol precursors and 6-endo bromoetherification of a bishomoallylic alcohol. In this paper, we report total assignments of their stereostructures through their asymmetric chemical syntheses and also their preliminary cytotoxic activities against some tumor cells. These results could not have been achieved without depending on asymmetric total synthesis.     

Normal approximation and fourth moment theorems for monochromatic triangles

Given a graph sequence denote by T₃(G_n) the number of monochromatic triangles in a uniformly random coloring of the vertices of G_n with colors. In this paper we prove a central limit theorem (CLT) for T₃(G_n) with explicit error rates, using a quantitative version of the martingale CLT. We then relate this error term to the well-known fourth-moment phenomenon, which, interestingly, holds only when the number of colors satisfies . We also show that the convergence of the fourth moment is necessary to obtain a Gaussian limit for any , which, together with the above result, implies that the fourth-moment condition characterizes the limiting normal distribution of T₃(G_n), whenever . Finally, to illustrate the promise of our approach, we include an alternative proof of the CLT for the number of monochromatic edges, which provides quantitative rates for the results obtained in [7].