“…In this context we have recently reported examples of double and triple ladders ( A , R = alkyl, X = Cl, OAc; B , X = Cl, R = CH 2 SiMe 3 ). − Their structures are related to the well-known single ladders (distannoxanes) C (R = alkyl, aryl, X = range of anions), which are useful as mild Lewis acid catalysts in a variety of organic reactions. − Interestingly, distannoxanes have not yet found utility in synthesis requiring chiral transformations, probably because no suitable chiral distannoxanes have yet been reported. Furthermore, distannoxanes undergo extensive dissociation in solution, a property that also reduces their potential as chiral information transfer reagents. − By contrast, double and triple ladders undergo fewer dissociation reactions in solution, but, significantly, in these cases chiral information is retained at the tin centers . A key motivation for our investigations has been the synthesis of new double ladders that have little or no symmetry as well as to increase the size of the interlayer region …”