Vineet Kumar Soni

Bio: Vineet Kumar Soni is an academic researcher from Indian Institute of Technology, Jodhpur. The author has contributed to research in topics: Catalysis & Radical cyclization. The author has an hindex of 9, co-authored 32 publications receiving 260 citations. Previous affiliations of Vineet Kumar Soni include Chung-Ang University & Indian Institute of Technology Delhi.

Generation of N-Centered Radicals via a Photocatalytic Energy Transfer: Remote Double Functionalization of Arenes Facilitated by Singlet Oxygen.

Abstract: An unprecedented approach to the generation of an N-centered radical via a photocatalytic energy-transfer process from readily available heterocyclic precursors is reported, which is distinctive of the previous electron transfer approaches. In combination with singlet oxygen, the in-situ-generated nitrogen radical from the oxadiazoline substrate in the presence of fac-Ir(ppy)3 undergoes a selective ipso addition to arenes to furnish remotely double-functionalized spiro-azalactam products. The mechanistic studies provide compelling evidence that the catalytic cycle selects the energy-transfer pathway. A concurrent activation of molecular oxygen to generate singlet oxygen by energy transfer is also rationalized. Furthermore, the occurrence of the electron transfer phenomenon is excluded on the basis of the negative driving forces for one-electron transfer between oxadiazoline and the excited state of fac-Ir(ppy)3 with a consideration of their redox potentials. The necessity of singlet oxygen as well as the photoactivated oxadiazoline substrate is clearly supported by a series of controlled experiments. Density functional studies have also been carried out to support these observations. The scope of substrates is explored by synthesizing diversely functionalized cyclohexadienone moieties in view of their utility in complex organic syntheses and as potential targets in pharmacology.

Reactivity Tuning for Radical–Radical Cross-Coupling via Selective Photocatalytic Energy Transfer: Access to Amine Building Blocks

Abstract: Reductive N–O bond cleavage has been widely explored for providing either N or O radical species for various coupling processes. Despite significant advances, this photoredox pathway is less appeal...

Ni/Co-Natural Clay as Green Catalysts for Microalgae Oil to Diesel-Grade Hydrocarbons Conversion

Abstract: The Ni/Co-natural clay catalysts have been prepared for the conversion of algae oil into diesel-grade hydrocarbons. Methyl oleate was used as a model compound for the present study. Ni/clay catalyst promotes decarboxylation/decarbonylation, whereas remarkable selectivity in hydrodeoxygenation (HDO) is achieved with Co/clay catalysts. Powder XRD and DRS studies of substrate mixed catalysts reveal a more prominent adsorption of substrate molecules over the Ni surface, which results in low HDO selectivity of nickel catalysts by surpassing the essential contribution of acidic sites. The HDO process provides higher carbon atom economy and energy value over decarboxylation/decarbonylation, while further reducing the formation of greenhouse gases such as CO2 and CH4. Total yield of saturated hydrocarbons from algae oil was 84–86 wt % with similar selectivity. The HDO rates of different fatty acids present in algae oil were independent of the fatty acid chain length. The catalysts are cost-effective and recyclabl...

Palladium-Nanoparticles-Intercalated Montmorillonite Clay: A Green Catalyst for the Solvent-Free Chemoselective Hydrogenation of Squalene

Abstract: Squalane is an important ingredient in the cosmetic, nutraceutical, and pharmaceutical industries. It has also been used as a model compound for the hydrocracking of crude and microalgae oil. Thus, a series of green heterogeneous metal catalysts were prepared to achieve complete hydrogenation of highly unsaturated squalene into squalane. Surface modification of the clay and metal intercalation simultaneously occurred during wet impregnation. The Pd-nanoparticles-intercalated clay with a dominating Pd(1 1 1) facet showed the highest reactivity and selectivity. The catalyst was stable with very low Pd leaching (≈0.03 ppm) and was recyclable without losing any significant catalytic activity.

Handbook of heterogeneous catalytic hydrogenation for organic synthesis

Abstract: Preface. Hydrogenation Catalysts. Reactors and Reaction Conditions. Hydrogenation of Alkenes. Hydrogenation of Alkynes. Hydrogenation of Aldehydes and Ketones. Preparation of Amines by Reductive Alkylation. Hydrogenation of Nitriles. Hydrogenation of Imines, Oximes, and Related Compounds. Hydrogenation of Nitro, Nitroso, and Related Compounds. Hydrogenation of Carboxylic Acids, Esters, and Related Compounds. Hydrogenation of Aromatic Compounds. Hydrogenation of Heterocyclic Aromatic Compounds. Hydrogenolysis. General Bibliography. Author Index. Subject Index.

Visible light photocatalysis in the late-stage functionalization of pharmaceutically relevant compounds.

Abstract: The late stage functionalization (LSF) of complex biorelevant compounds is a powerful tool to speed up the identification of structure-activity relationships (SARs) and to optimize ADME profiles. To this end, visible-light photocatalysis offers unique opportunities to achieve smooth and clean functionalization of drugs by unlocking site-specific reactivities under generally mild reaction conditions. This review offers a critical assessment of current literature, pointing out the recent developments in the field while emphasizing the expected future progress and potential applications. Along with paragraphs discussing the visible-light photocatalytic synthetic protocols so far available for LSF of drugs and drug candidates, useful and readily accessible synoptic tables of such transformations, divided by functional groups, will be provided, thus enabling a useful, fast, and easy reference to them.

Photoinduced intermolecular hydrogen atom transfer reactions in organic synthesis

Abstract: Summary Hydrogen-atom transfer (HAT) provides straightforward methods to generate open-shell radical intermediates from R-H (R = C, Si, etc.) bonds and offers unique opportunities for green and sustainable synthesis. Traditional HAT protocols required harsh conditions and relied on the use of harmful reagents such as Cl2 and peroxides. An emerging strategy is photoinduced intermolecular HAT, in which transformations can be driven by photocatalysis under mild conditions. In recent years, photoinduced intermolecular HAT reactions have seen substantial development of their versatility, efficiency, and selectivity. This review summarizes recent advances (up to December 2020) in this rapidly expanding research area. The representative examples provided are classified according to the active species responsible for hydrogen atom abstraction. The reactivity, selectivity, and established transformations for each type of active species are briefly summarized. This review aims to provide guidance for the application of photoinduced HAT in R-H functionalization reactions and to inspire further progress in this research area.

Stereoselective and Versatile Preparation of Tri- and Tetrasubstituted Allylic Amine Scaffolds under Mild Conditions

Abstract: Significant progress has been observed in recent years in the synthesis of allylic amines, which are important building blocks in synthetic chemistry. Most of these processes are effective toward the preparation of allylic amines, with limited potential to introduce three or four different substituents on the olefinic unit in a stereocontrolled fashion. Therefore, the discovery of a mild and operationally simple protocol allowing such challenging stereoselective synthesis of multisubstituted allylic amines remains an inspiring target. Herein, we report the first general and practical methodology for the stereoselective synthesis of tri- and tetrasubstituted allylic amines based on Pd-catalyzed conversion of allyl surrogates readily obtained from cyclic vinyl carbonates. These rare conversions are characterized by excellent stereoselectivity, operational simplicity, mild reaction conditions, and wide scope in reaction partners. DFT studies were performed to rationalize the stereocontrol in these allylic am...

Strategies to Generate Nitrogen-centered Radicals That May Rely on Photoredox Catalysis: Development in Reaction Methodology and Applications in Organic Synthesis.

Abstract: For more than 70 years, nitrogen-centered radicals have been recognized as potent synthetic intermediates. This review is a survey designed for use by chemists engaged in target-oriented synthesis. This review summarizes the recent paradigm shift in access to and application of N-centered radicals enabled by visible-light photocatalysis. This shift broadens and streamlines approaches to many small molecules because visible-light photocatalysis conditions are mild. Explicit attention is paid to innovative advances in N-X bonds as radical precursors, where X = Cl, N, S, O, and H. For clarity, key mechanistic data is noted, where available. Synthetic applications and limitations are summarized to illuminate the tremendous utility of photocatalytically generated nitrogen-centered radicals.