Results 231 to 240 of about 23,430 (289)

Bioresorbable Scaffolds for Coronary Arteries: Where Do We Stand Today?

open access: yesVIEW Medicine, Volume 1, Issue 1, August 2026.
Bioresorbable coronary scaffolds are moving from thick strut pitfalls to thinner, stronger, healing‐oriented designs. Integrating advances in materials, guided implantation with preparation, size, and postdilation steps, and resorption aligned to healing, we synthesize clinical evidence and chart a roadmap toward intelligent, transient platforms ...
Junya Matsuda   +5 more
wiley   +1 more source

Catalytic Asymmetric Hydration of Alkenes. [PDF]

open access: yesJ Am Chem Soc
Hatano H   +13 more
europepmc   +1 more source

Orthogonal One‐Pot Dual Catalysis Enabled by a Hybrid Chiral Diene/Phosphine Ligand

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 14, 17 July 2026.
A hybrid chiral diene–phosphine ligand enables orthogonal one‐pot Rh/Pd relay catalysis, delivering high yields and enantioselectivities while outperforming dual‐ligand systems. A hybrid chiral diene‐phosphine ligand (L1) enables orthogonal one‐pot relay catalysis by integrating distinct metal‐coordination sites within a single molecular framework. The
Steven Jiménez‐Guailla   +2 more
wiley   +1 more source

Sustainable Synthesis of Bio‐Based Furanic and Aromatic Amines Using an Optimized Whole‐Cell Transaminase–Decarboxylase Cascade in E. coli RARE

open access: yesChemBioChem, Volume 27, Issue 13, 14 July 2026.
A whole‐cell biocatalytic cascade in engineered Escherichia coli RARE couples the ω‐transaminase from Pseudomonas psychrotolerans with pyruvate decarboxylase from Zymomonas mobilis to shift transamination toward amine formation via pyruvate removal. Integration of the cascade into a chemo‐enzymatic synthesis pathway enables the scalable production of 2,
Laura Edit Barabás   +5 more
wiley   +1 more source

Structure-Guided Discovery of Selective Polo-Like Kinase 3 Inhibitors. [PDF]

open access: yesACS Med Chem Lett
Yap JL   +26 more
europepmc   +1 more source

Fluorinated Aminopiperidones as Non‐Glutarimide Thalidomide Analogs: Stereodivergent Synthesis and Validation

open access: yesChemMedChem, Volume 21, Issue 13, 14 July 2026.
Fluorinated aminopiperidones, designed as non‐glutarimide thalidomide analogs, were synthesized with full regio‐ and stereocontrol. The C*–CF3 used as carbonyl surrogate improved solubility and membrane interactions while abolishing cereblon binding.
Boštjan Adamlje   +11 more
wiley   +1 more source

An Ugi–Joullié Platform for Medicinally Relevant 1,4‐Dihydrobenzothiazines

open access: yesChemMedChem, Volume 21, Issue 13, 14 July 2026.
A series of benzothiazine derivatives was efficiently synthesized via an UJ‐2CR of a preformed imine and diverse isocyanides. The method features mild, room‐temperature conditions, broad functional‐group tolerance, and scalability, enabling rapid access to a chemically diverse library of 19 adducts with potential for further medicinal chemistry ...
Xiaofang Lei   +9 more
wiley   +1 more source

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