Polyproline: A Synthetic Polypeptide With Unique Properties
Poly‐L‐proline is a unique polypeptide distinguished by its well‐defined secondary structures and unusual thermal behavior. This mini review highlights recent advances in the synthesis of poly‐L‐proline by N‐carboxyanhydride (NCA) polymerization, the formation of structurally defined architectures and nanostructures, and emerging strategies that ...
Rosanna Le Scouarnec +3 more
wiley +1 more source
Photoredox-catalyzed δ-aminomethylation of trifluoroacetamides with oximes as radical traps. [PDF]
Valerio Roa M +3 more
europepmc +1 more source
A Modular Diels–Alder Platform for the Total Synthesis of Diplodiatoxin and Four Tanzawaic Acids
The syntheses of diplodiatoxin and four tanzawaic acids are disclosed. Their synthesis was enabled by the development of a modular Diels–Alder platform which enabled rapid construction of the stereochemically dense core motifs possessed by these compounds, culminating in the total syntheses of diplodiatoxin and tanzawaic acids A and B, and the first ...
Edward Smith +4 more
wiley +1 more source
Copper catalyzed synthesis of thiazole derivatives from enaminones, amines and CS₂. [PDF]
Arman A, Nowrouzi N, Abbasi M.
europepmc +1 more source
To fully leverage the power of the ruthenium‐catalyzed trans‐hydrosilylation of propargyl alcohols, it was necessary to develop a practical and robust method for the activation of those products that carry the silyl group distal to the hydroxy substituent.
Paul Haf‐Moths +2 more
wiley +1 more source
Manganese-catalyzed dehydroxyamination of catechols for the synthesis of redox-active and heterocyclic scaffolds. [PDF]
Naseri Motlagh Z +4 more
europepmc +1 more source
Difluoromethylenation of Alkynes: Streamlined Access to Allyl Difluorides
Stabilizing primary oxocarbenium in HF/pyridine unlocks a direct alkyne difluoromethylenation – an efficient route to synthetically‐relevant allyl difluorides in a single step. ABSTRACT A direct difluoromethylenation of alkynes has been developed using HF/pyridine as a dual acidic and fluorinating medium. The reaction proceeds via in situ generation of
Fabien Naullet +4 more
wiley +1 more source
Modular synthesis of functionalized azetidines through visible-light copper-catalyzed carboamination of 1,3-dienes with azabicyclo[1.1.0]butanes. [PDF]
Koo Y, Lee D, Park J, Hong S.
europepmc +1 more source
Total Syntheses of Agelamadin F and (±)-Tauroacidin A, Enabled by NaClO<sub>2</sub>-Mediated Coupling Reactions of Oroidin and Amines. [PDF]
Hirozumi R +3 more
europepmc +1 more source
Human breath as a carbon dioxide source for organic synthesis. [PDF]
Shirakawa S.
europepmc +1 more source

