C–H functionalization of pyridines
S Maity, A Bera, A Bhattacharjya, P Maity - Organic & Biomolecular …, 2023 - pubs.rsc.org
Pyridine and its reduced form (piperidine) are the most common nitrogen heterocycles in
FDA-approved drugs. Additionally, their presence in alkaloids, ligands for transition metals …
FDA-approved drugs. Additionally, their presence in alkaloids, ligands for transition metals …
Diversely functionalized isoquinolines and their core-embedded heterocyclic frameworks: a privileged scaffold for medicinal chemistry
A Vijayakumar, M Manod, RB Krishna… - RSC Medicinal …, 2023 - pubs.rsc.org
Isoquinoline-enrooted organic small-molecules represent a challenging molecular target in
the organic synthesis arsenal attributed of its structural diversity and therapeutic importance …
the organic synthesis arsenal attributed of its structural diversity and therapeutic importance …
Organophosphites: An addition to the arsenal of organocatalysts
Organophosphites are nucleophilic in nature and can act as a good leaving group owing to
the stability of the phosphite anion. This dual reactivity makes them good candidates for …
the stability of the phosphite anion. This dual reactivity makes them good candidates for …
In-cage recombination facilitates the enantioselective organocatalytic [1, 2]-rearrangement of allylic ammonium ylides
The [1, 2]-rearrangement of allylic ammonium ylides is traditionally observed as a
competitive minor pathway alongside the thermally allowed [2, 3]-sigmatropic …
competitive minor pathway alongside the thermally allowed [2, 3]-sigmatropic …
Phosphite mediated molecular editing via switch to meta-C–H alkylation of isoquinolines: emergence of a distinct photochemical [1, 3] N to C rearrangement
The isoquinoline core is present in one of the largest subsets of bioactive natural products.
The multifunctional isoquinoline core exerts diverse bioactivity, resulting in the development …
The multifunctional isoquinoline core exerts diverse bioactivity, resulting in the development …
The Enantioselective Organocatalytic [1, 2]-Rearrangement of Allylic Ammonium Ylides
The [1, 2]-rearrangement of allylic ammonium ylides is traditionally observed as a
competitive minor pathway alongside the thermally allowed [2, 3]-sigmatropic …
competitive minor pathway alongside the thermally allowed [2, 3]-sigmatropic …
[ЦИТИРОВАНИЕ][C] The Wittig Rearrangement
JP Wolfe, AR Perez - 2024 - Elsevier