Results 201 to 210 of about 136,021 (344)
The brittleness of PLimC, which is made from limonene oxide and CO2 remains a challenge for applications. The terpolymerization of trans‐limonene oxide (LimO), trans‐menth‐1‐ene oxide (Men1O), and CO2 was shown to yield a platform for tailored graft copolymerization and was transformed into a macroinitiator for atom transfer radical polymerization ...
Marcel Höferth+2 more
wiley +1 more source
RefAHL: a curated quorum sensing reference linking diverse LuxI-type signal synthases with their acyl-homoserine lactone products. [PDF]
Schaefer AL+5 more
europepmc +1 more source
On the Bouveault-Locquin's Lactone-Trimethylenering-Rearrangement
松井 正直, 平瀬 進
openalex +2 more sources
Terpenes and Terpenoids: How can we use them?
The transition from petroleum‐based to renewable bio‐based chemicals has led to increased interest in terpenes and terpenoids. This overview highlights their chemistry, focusing on their reactivity and applications in polymerizations, total syntheses, pharmaceuticals, and bio‐based chemical conversions; promoting sustainable and green chemical ...
Jay Hanssens+3 more
wiley +1 more source
Stereocontrolled synthesis of 3-hydroxy-2-piperidinone carboxamides by catalytic ring-opening aminolysis of bridged <i>δ</i>-lactam-γ-lactones. [PDF]
Beng TK+4 more
europepmc +1 more source
Synthesis of
F. A. Isherwood+2 more
openalex +1 more source
The reaction of 2‐hydroxycyclobutanone with a Wittig reagent bearing a benzooxazolone moiety results in the formation of a cyclobutane‐fused bicyclic γ‐lactone with the heterocyclic unit located at the bridgehead position. The proposed mechanism involves the transfer of the acyl ylide fragment and an intramolecular Wittig reaction to provide an ...
Stefano Barranco+6 more
wiley +1 more source
Synthesis of bicyclo[3.2.0]heptane lactones <i>via</i> a ligand-enabled Pd-catalyzed C(sp<sup>3</sup>)-H activation cascade. [PDF]
Fan Z, Cai X, Sheng T, Yu JQ.
europepmc +1 more source
Total Synthesis of Ectocarpin A
A fully enantioselective total synthesis of ectocarpin A, a new oxylipin, has been achieved in 12 steps starting from tetrahydro‐1H‐cyclopentafuranone. Key steps include the formation of the chiral core, diastereoselective epoxidation, enzymatic desymmetrization of a 1,4‐diol, epimerization, and strategic Wittig and Julia‐Kocienski olefinations to ...
Alexandre Guy+2 more
wiley +1 more source