Enantioselective Aziridination of Unactivated Terminal Alkenes Using a Planar Chiral Rh(III) Indenyl Catalyst.

Chiral aziridines are important structural motifs found in natural products and various target molecules. They serve as versatile building blocks for the synthesis of chiral amines. While advances in catalyst design have enabled robust methods for enantioselective aziridination of activated olefins, simple and abundant alkyl-substituted olefins pose a significant challenge. In this work, we introduce a novel approach utilizing a planar chiral rhodium indenyl catalyst to facilitate the enantioselective aziridination of unactivated alkenes. This transformation exhibits a remarkable degree of functional group tolerance and displays excellent chemoselectivity favoring unactivated alkenes over their activated counterparts, delivering a wide range of enantioenriched high-value chiral aziridines. Computational studies unveil a stepwise aziridination mechanism in which alkene migratory insertion plays a central role. This process results in the formation of a strained four-membered metallacycle and serves as both the enantio- and rate-determining steps in the overall reaction.

Metal-Ligand Cooperativity to Assemble a Neutral and Terminal Niobium Phosphorus Triple Bond (Nb≡P).

Decarbonylation along with P-atom transfer from the phosphaethynolate anion, PCO- , to the NbIV complex [(PNP)NbCl2 (Nt BuAr)] (1) (PNP=N[2-Pi Pr2 -4-methylphenyl]2 - ; Ar=3,5-Me2 C6 H3 ) results in its coupling with one of the phosphine arms of the pincer ligand to produce a phosphanylidene phosphorane complex [(PNPP)NbCl(Nt BuAr)] (2). Reduction of 2 with CoCp*2 cleaves the P-P bond to form the first neutral and terminal phosphido complex of a group 5 transition metal, namely, [(PNP)Nb≡P(Nt BuAr)] (3). Theoretical studies have been used to understand both the coupling of the P-atom and the reductive cleavage of the P-P bond. Reaction of 3 with a two-electron oxidant such as ethylene sulfide results in a diamagnetic sulfido complex having a P-P coupled ligand, namely [(PNPP)Nb=S(Nt BuAr)] (4).

Correlation between Collagen Type I/III Ratio and Scar Formation in Patients Undergoing Immediate Reconstruction with the Round Block Technique after Breast-Conserving Surgery.

The aim of this study was to investigate the relationship between the collagen type I/III ratio and scarring in patients who underwent immediate reconstruction with the round block technique (RBT) after breast conservation surgery. Seventy-eight patients were included, and demographic and clinical characteristics were recorded. The collagen type I/III ratio was measured using immunofluorescence staining and digital imaging, and scarring was assessed using the Vancouver Scar Scale (VSS). The mean VSS scores were 1.92 ± 2.01 and 1.79 ± 1.89, as assessed by two independent plastic surgeons, with good reliability of the scores. A significant positive correlation was found between VSS and the collagen type I/III ratio (r = 0.552, p < 0.01), and a significant negative correlation was found between VSS and the collagen type III content (r = -0.326, p < 0.05). Multiple linear regression analysis showed that the collagen type I/III ratio had a significant positive effect on VSS (ß = 0.415, p = 0.028), whereas the collagen type I and collagen type III content had no significant effect on VSS. These findings suggest that the collagen type I/III ratio is associated with scar development in patients undergoing RBT after breast conservation surgery. Further research is needed to develop a patient-specific scar prediction model based on genetic factors affecting the collagen type I/III ratio.

Ligand non-innocence allows isolation of a neutral and terminal niobium nitride.

Complex (PNP)NbCl2(N[tBu]Ar) (1) (PNP- = N[2-PiPr2-4-methylphenyl]2; Ar = 3,5-Me2C6H3) reacts with one equiv. of NaN3 to form a mixture of (PNPN)NbCl2(N[tBu]Ar) (2) and (PNP)NbN(N[tBu]Ar) (3), both of which have been spectroscopically and crystallographically characterized, including 15N isotopic labelling studies. Complex 3 represents the first structurally characterized example of a neutral and mononuclear Nb nitride. Independent studies established 3 to form via two-electron reduction of 2, whereas oxidation of 3 by two-electrons reversed the process. Computational studies suggest the transmetallation step to produce the intermediate [(PNP)NbCl(N3)(N[tBu]Ar)] (A) which extrudes N2 to form the phosphinimide [(PNPN)NbCl(N[tBu]Ar)] (B) followed by disproportionation to 2 and low-valent [(PNPN)Nb(N[tBu]Ar)] (C). The latter then undergoes intramolecular N-atom transfer to form the nitride moiety in 3.