Bite angle

Enantioselective synthesis

Catalysis

Denticity

Organic chemistry

Chemistry

Amination

Combinatorial chemistry

Tsuji–Trost reaction

Diphosphines

Metal

Stereochemistry

Transition state

Accounts of Chemical Research

ConspectusWhile spectacular successes have been achieved in homogeneous catalysis with the use of achiral diphosphine ligands featuring a wide natural bite angle, such as XantPhos, chiral diphosphines that can induce a large P–M–P bite angle in their transition metal complexes are conspicuously less explored in asymmetric catalysis, probably due to the challenges in the identification and efficient construction of a suitable chiral backbone. In the past decade, a highly efficient synthesis of chiral aromatic spiroketals and the corresponding diphosphine ligands (SKPs) has been developed in this group.Based on a one-pot catalytic tandem double asymmetric hydrogenation–spiroketalization ring-closure reaction sequence, these SKP ligands featuring an extraordinarily long P···P distance and a flexible backbone have been readily prepared in large scale. Remarkably versatile coordination modes have been found in the complexes of SKP with some catalysis-relevant transition metals, for example, Pd, Cu, Au, and Rh. Whereas SKP enforces an unusually large bite angle in [Pd(SKP)Cl2] and [Cu(SKP)Cl] complexes (160.1° and 132.8°, respectively), it also allows for a bimetallic Au–Au interaction (3.254 Å) in the complex of [Au2(SKP)Cl2] or a square-planar coordination geometry for the [Rh(SKP)(cod)]SbF6 complex. Such an adaptable nature of SKP ligands for transition metal coordination has profound consequences in homogeneous asymmetric catalysis, as demonstrated by their unique performance in several types of catalytic asymmetric reactions. One of the most exciting examples is SKP/Pd-catalyzed asymmetric allylic amination of Morita–Baylis–Hillman (MBH) adducts, in which SKP/Pd complexes demonstrated excellent control of regio- and enantioselectivities and exhibited exceptionally high efficiency (with a TON up to 4750) in the catalysis. SKP ligands have also found a diversity of successful applications in Cu-, Au-, or Rh-catalyzed asymmetric reactions, further attesting their wide utilities in asymmetric catalysis. Overall, this class of readily accessible SKP ligands featuring a chiral aromatic spiroketal skeleton have demonstrated unique adaptable structures in a variety of transition metal complexes and provided outstanding performance in some difficult asymmetric transformations. The works delineated herein would be expected to stimulate further research efforts on the application of this type of chiral ligand and to provide useful clues in the design of new chiral diphosphine ligands with adaptable bite angles for transition metal catalyzed asymmetric reactions.

A Type of Structurally Adaptable Aromatic Spiroketal Based Chiral Diphosphine Ligands in Asymmetric Catalysis