Category: 3393-45-1

Name: 5,6-Dihydro-2H-pyran-2-one. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 5,6-Dihydro-2H-pyran-2-one, is researched, Molecular C5H6O2, CAS is 3393-45-1, about Synthesis of Pyrroles via Consecutive 6π-Electrocyclization/Ring-Contraction of Sulfilimines. Author is Haut, Franz-Lucas; Feichtinger, Niklas J.; Plangger, Immanuel; Wein, Lukas A.; Mueller, Mira; Streit, Tim-Niclas; Wurst, Klaus; Podewitz, Maren; Magauer, Thomas.

Authors present a modular, synthetic entry to polysubstituted pyrroles employing readily available 2,5-dihydrothiophenes. Ring-opening of the heterocycle provides access to a panel of 1,3-dienes which underwent pyrrole formation in the presence of inexpensive chloramine-T trihydrate. The transformation is conducted in an open flask and proceeds at ambient temperatures (23°) in nondry solvents. A careful adjustment of the electronics and sterics of the 1,3-diene precursor allows for the isolation of key intermediates. DFT studies identified a reaction mechanism that features a 6π-electrocyclization of a sulfilimine intermediate followed by spontaneous ring-contraction to reveal the pyrrole skeleton.

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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Product Details of 3393-45-1. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 5,6-Dihydro-2H-pyran-2-one, is researched, Molecular C5H6O2, CAS is 3393-45-1, about Nucleophilic halo-Michael addition under Lewis-base activation. Author is Laina-Martin, Victor; Perez, Ignacio; Fernandez-Salas, Jose A.; Aleman, Jose.

A simple and general conjugate nucleophilic halogenation is presented. The THTO/halosilane combination has shown the ability to act as a nucleophilic halide source in the conjugate addition to a variety of Michael acceptors. In addition, a straightforward diastereoselective halogen installation using α,β-unsaturated acyloxazolidinones as platforms has been developed.

If you want to learn more about this compound(5,6-Dihydro-2H-pyran-2-one)Product Details of 3393-45-1, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(3393-45-1).

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Novel multi-dentate phosphines for Pd-catalyzed alkoxycarbonylation of alkynes promoted by H2O additive, published in 2019-03-31, which mentions a compound: 3393-45-1, Name is 5,6-Dihydro-2H-pyran-2-one, Molecular C5H6O2, Application In Synthesis of 5,6-Dihydro-2H-pyran-2-one.

A series of novel multi (bi-/tri-/tetra-)-dentate phosphines with good robustness against water and oxygen were synthesized and fully characterized. It was found that the developed ionic tri-dentate phosphine enabled Pd-catalyzed alkoxycarbonylation of alkynes with CO and alcs. which gave α,β-unsaturated esters RCH=CHCO2R1 [R = n-Bu, Ph, Bn, etc.; R1 = Me, Et, i-Pr, C6H11] and I using H2O as an additive instead of acid. As for ionic tri-dentate phosphine, its unique steric configuration with two types of potential P-P chelation modes (P···P distance of 4.31 Å and 4.36 Å resp.) to Pd-center rendered the corresponding Pd-catalyst high activity and good stability for alkoxycarbonylation of alkynes. The in situ FT-IR anal. also verified that the formation and stability of Pd-H active species were greatly facilitated with the presence of ionic tri-dentate phosphine as well as H2O additive. In addition, as an ionic phosphine, ionic tri-dentate phosphine based PdCl2(MeCN)2 system immobilized in RTIL of [Bmim]NTf2 could be recycled for 7 runs without obvious activity loss or metal leaching.

Here is a brief introduction to this compound(3393-45-1)Application In Synthesis of 5,6-Dihydro-2H-pyran-2-one, if you want to know about other compounds related to this compound(3393-45-1), you can read my other articles.

Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI