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Boronate assemblies

Unless there is a chiral ligand on boron, assemblies a and b of Scheme 5.2 are enantiomeric and the product will be racemic. If the ligand is chiral, then the transition structures are diastereomeric and the products will be formed in unequal amounts under conditions of kinetic control (Chapter 1). Figure 5.1 illustrates several chiral boron reagents that have been tested in the allyl boration reaction, with typical enantioselectivities for each. [Pg.163]

Assemblies relying on the dative B-N interaction in conjunction with boronate ester formation to form linear polymers have also been identified. Unlike the stepwise phenanthroline-boronate assembly, esterification coupled with ligation occurs simultaneously. In fact, it is likely that coordination... [Pg.267]


See other pages where Boronate assemblies is mentioned: [Pg.255]    [Pg.255]    [Pg.257]    [Pg.257]    [Pg.259]    [Pg.261]    [Pg.263]    [Pg.267]    [Pg.269]    [Pg.270]    [Pg.271]    [Pg.273]    [Pg.275]    [Pg.277]    [Pg.279]    [Pg.281]    [Pg.283]    [Pg.285]    [Pg.287]   


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Amides, boronate assemblies

Amines boronate assemblies

Boronate assemblies characterized

Boronate assemblies coordination-based macrocyclic

Boronate assemblies covalently linked

Boronate assemblies types

Boronic acids polymer self-assembly

Boronic acids self-assembly

Boronic supramolecular assemblies

Carbon boronate assemblies

Esters, boronate assemblies

Hydrogen bonds/bonding boronate assemblies

Imine, boronate assemblies

Kinetics boronate assemblies

Linked Boronate Assemblies

Macrocyclic assemblies boronate

Polymer Self-Assembly Mediated by Boronic Acid

Supramolecular Boronate Assemblies

Water boronate assemblies

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