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We develop and analyze a model for the interaction of a quasi-Newtonian free fluid with a poroelastic medium. The flow in the fluid region is described by the nonlinear Stokes equations and in the poroelastic medium by the nonlinear quasi-static Biot model. Equilibrium and kinematic conditions are imposed on the interface. We establish existence and uniqueness of a solution to the weak formulation and its semidiscrete continuous-in-time finite element approximation. We present error analysis, complemented by numerical experiments. 

Organocatalysis has emerged as a powerful synthetic tool in organic chemistry in the last few decades. Among various classes of organocatalysis, chiral diol-based scaffolds, such as BINOLs, VANOLs, and tartaric acid derivatives, have been widely used to induce enantioselectivity due to the ability of the hydroxyls to coordinate with the Lewis acidic sites of reagents or substrates and create a chiral environment for the transformation. In this review, we will discuss the applications of these diol-based catalysts in different types of reactions, including the scopes of reactions and the modes of catalyst activation. In general, the axially chiral aryl diol BINOL and VANOL derivatives serve as the most competent catalyst for most examples, but examples of exclusive success using other scaffolds, herein, suggests that they should not be overlooked. Lastly, the examples, to date, are mainly from tartrate and biaryl diol catalysts, suggesting that innovation may be available from new diol scaffolds.