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• Swollen-induced in-situ encapsulation of catalysts in cross-linked polysiloxane elastomers polymer. • Silicone rubber-based microchannel reactor was employed for asymmetric transforms. • Cross-linked polysiloxane elastomers was proved to be easily recycled by filtration or pick-up,reused by several times and exhibits excellent enantioselectivities 94–96% ees The immobilization of molecular catalysts to fabricate heterogeneous catalysts for catalytic asymmetric transformations is extremely important and has attracted great attentions. Herein we developed a simple and new strategy for the heterogenization of homogeneous molecular complexes into the cross-linked polymer. It is demonstrated for the first time that the cross-linked polysiloxane elastomers can be applied for the swollen-induced in-situ encapsulation of homogeneous catalysts with or without chiral ligands. The swollen-induced in-situ encapsulation of silver catalyst system in the cross-linked polysiloxane elastomers led to the formation of silicone rubber-based hierarchically porous that could be used in asymmetric [3+2] cycloaddition, asymmetric tandem conjugate addition−elimination reaction and oxidation of hydrosilanes to silanols. The swollen-induced in-situ encapsulation of chiral silver complex in the cross-linked polysiloxane elastomers was proved to be easily recycled by filtration or pick-up and reused by several times. The simplest heterogeneous catalysis by the strategy of swollen-induced in-situ encapsulation can be extended to the encapsulation of chiral metal catalysts into different polymeric materials for the heterogenization of homogeneous catalysis. [Display omitted] [ABSTRACT FROM AUTHOR]

A unique 1,3-dipolar [3+2] cycloaddition of alkyl 4-oxo-4-arylbut-2-enoates bearing two different electron-withdrawing groups was completed by using the silver/(R)-DTBM-Segphos catalyst system, which gives the corresponding fully substituted pyrrolidines with four stereogenic centers in good yields and with excellent enantioselectivities (up to 98% ee). [ABSTRACT FROM AUTHOR]

A novel and unusual palladium‐catalyzed [4+2] annulation of cyclopropenes with benzosilacyclobutanes is reported. This reaction occurred through chemoselective Si−C(sp2) bond activation in synergy with ring expansion/insertion of cyclopropenes to form new C(sp2)−C(sp3) and Si−C(sp3) bonds. An array of previously elusive bicyclic skeleton with high strain, silabicyclo[4.1.0]heptanes, were formed in good yields with excellent diastereoselectivity under mild conditions. An asymmetric version of the reaction with a chiral phosphoramidite ligand furnished a variety of chiral bicyclic silaheterocycle derivatives with good enantioselectivity (up to 95.5:4.5 er). Owing to the mild reaction conditions, the good stereoselectivity profile, and the ready availability of the functionalized precursors, this process constitutes a useful and straightforward strategy for the synthesis of densely functionalized silacycles. [ABSTRACT FROM AUTHOR]

A novel and unusual palladium‐catalyzed [4+2] annulation of cyclopropenes with benzosilacyclobutanes is reported. This reaction occurred through chemoselective Si−C(sp2) bond activation in synergy with ring expansion/insertion of cyclopropenes to form new C(sp2)−C(sp3) and Si−C(sp3) bonds. An array of previously elusive bicyclic skeleton with high strain, silabicyclo[4.1.0]heptanes, were formed in good yields with excellent diastereoselectivity under mild conditions. An asymmetric version of the reaction with a chiral phosphoramidite ligand furnished a variety of chiral bicyclic silaheterocycle derivatives with good enantioselectivity (up to 95.5:4.5 er). Owing to the mild reaction conditions, the good stereoselectivity profile, and the ready availability of the functionalized precursors, this process constitutes a useful and straightforward strategy for the synthesis of densely functionalized silacycles. [ABSTRACT FROM AUTHOR]

Frontispiz: Controllable Si-C Bond Activation Enables Stereocontrol in the Palladium-Catalyzed [4+2] Annulation of Cyclopropenes with Benzosilacyclobutanes Keywords: Gespannte Moleküle; Palladium; Ringaufweitung; Si-C-Bindungsaktivierung; Silacyclen Gespannte Moleküle, Palladium, Ringaufweitung, Si-C-Bindungsaktivierung, Silacyclen. [Extracted from the article]