Search Results - "Philip, Rose Mary"

Nickel catalysts in Sonogashira coupling reactions by Nair, Pravya P, Philip, Rose Mary, Anilkumar, Gopinathan

“…Nickel has emerged as a desirable substitute for palladium in Sonogashira coupling reactions due to its abundance, less toxicity and high catalytic activity…”
Get more information

A novel manganese/iodine-catalyzed Ortoleva-King type protocol for the synthesis of imidazo[1,2-a]pyridines and Zolimidine by Aneeja, Thaipparambil, Mary Philip, Rose, Anilkumar, Gopinathan

“…[Display omitted] •The first manganese-iodine catalyzed Ortoleva-King type protocol for the synthesis of imidazo[1,2-a]pyridines.•This protocol employs readily…”
Get full text

Silver-catalysed decarboxylative cross-couplings by Shaji Anand, Neelakandan, Mary Philip, Rose, Anilkumar, Gopinathan

Get full text

Low‐Cost Transition Metal‐Catalyzed Heck‐Type Reactions: An Overview by Alisha, Mathews, Philip, Rose Mary, Anilkumar, Gopinathan

“…Heck coupling has emerged as an effective and powerful tool for C−C bond formations, with applications in academic and industrial grounds. The conventional…”
Get full text

Recent Trends and Prospects in Homogeneous Manganese‐Catalysed Epoxidation by Philip, Rose Mary, Radhika, Sankaran, Abdulla, C. M. Afsina, Anilkumar, Gopinathan

“…Epoxidation of alkenes is a significant reaction in organic chemistry due to its opportunities in producing compounds of biochemical interest. Catalytic…”
Get full text

Nickel‐Catalysed Amination of Arenes and Heteroarenes by Philip, Rose Mary, Veetil Saranya, Padinjare, Anilkumar, Gopinathan

“…C(sp2)−N cross‐coupling is one of the most powerful transformations in organic synthesis to construct highly ubiquitous anilines and aniline derivatives. The…”
Get full text

Advances in non‐palladium‐catalysed Stille couplings by Aleena, Mary Baby, Philip, Rose Mary, Anilkumar, Gopinathan

“…Stille coupling is regarded as a powerful tool in the synthesis of a wide range of functionalised C–C bonds due to the high stability, availability and broad…”
Get full text

Recent advances and trends in the biomimetic iron‐catalyzed asymmetric epoxidation by Radhika, Sankaran, Aneeja, Thaipparambil, Philip, Rose Mary, Anilkumar, Gopinathan

“…Enantiomerically pure epoxides are extremely beneficial structural scaffolds in synthetic organic and medicinal chemistry. Complexes based on iron with ligands…”
Get full text

Applications of tert -butanesulfinamide in the synthesis of N-heterocycles via sulfinimines by Philip, Rose Mary, Radhika, Sankaran, Saranya, P V, Anilkumar, Gopinathan

“…Chiral sulfinamides are among the best known chiral auxiliaries in the stereoselective synthesis of amines and their derivatives. The most extensively used…”
Get full text

Applications of aryl-sulfinamides in the synthesis of N-heterocycles by Philip, Rose Mary, Treesa, G. S. Susan, Saranya, Salim, Anilkumar, Gopinathan

“…Enantiopure aryl-sulfinamides are important chiral auxiliaries in the asymmetric synthesis of amines and their derivatives. Here, we provide an overview of…”
Get full text

Recent advances and prospects in the Zn-catalysed Mannich reaction by Shamna, Salahudeen, Afsina, C. M. A, Philip, Rose Mary, Anilkumar, Gopinathan

“…Zn-catalysed reactions are ubiquitously important due to their inexpensive, generally less toxic and atom-economic nature. According to the modern criteria of…”
Get full text

Nickel/iodine-catalyzed synthesis of 2-arylimidazo[1,2-a]pyridines through Ortoleva-King type protocol by Philip, Rose Mary, Aneeja, Thaipparambil, Anilkumar, Gopinathan

“…[Display omitted] A novel Ni-I2 catalytic system was introduced for the synthesis of 2-arylimidazo[1,2-a]pyridines from readily available arylmethyl ketones…”
Get full text

Nickel catalyzed hydroamination reactions: An overview by Yamuna, Purushothaman, Philip, Rose Mary, Anilkumar, Gopinathan

“…Hydroamination is a valuable method for the synthesis of synthetically relevant nitrogen-containing compounds including amines, imines or enamines. Owing to…”
Get full text

Highly Regio- and Stereoselective Intramolecular Rearrangement of Glycidol Acetal to Alkoxy Cyclic Acetals by Johny, Meera, Philip, Rose Mary, Rajendar, Goreti

“…A new class of highly regio- and stereoselective intramolecular rearrangements of glycidol acetals to produce alkoxylated 1,3-dioxolane/1,3-dioxane is…”
Get full text

An overview of rhodium-catalysed heck type reactions by Alisha, Mathews, Philip, Rose Mary, Anilkumar, Gopinathan

“…•The first review on Rh-Catalysed Heck type reactions.•Environmentally benign couplings with reports in green solvents.•Wide applicability in natural product…”
Get full text

Synthesis of imidazo[1,2-a]pyridines via cobalt/iodine-catalyzed Ortoleva-King type approach by Saranya, Padinjare Veetil, Philip, Rose Mary, Anilkumar, Gopinathan

“…[Display omitted] •Ortoleva-King type reaction of 2-aminopyridines with easily available aromatic ketones.•Use of dual catalytic system of cobalt and…”
Get full text

Recent advances and prospects in the cobalt-catalyzed amination reactions by Saranya, Padinjare Veetil, Neetha, Mohan, Philip, Rose Mary, Anilkumar, Gopinathan

“…In the pharmaceutical industry, the amino group plays a crucial role in the production of molecules with interesting biological activity. Because of their…”
Get full text

Nickel-catalyzed (hetero)aryl borylations: an update by Mole, Julie, Philip, Rose Mary, Anilkumar, Gopinathan

Get full text

Synthesis of 2‐Aminobenzothiazoles via Nickel‐Catalyzed Tandem Reaction of 2‐Bromophenylisothiocyante with Amines by Philip, Rose Mary, Saranya, Padinjare Veetil, Anilkumar, Gopinathan

“…A tandem strategy for the synthesis of 2‐aminobenzothiazoles from 2‐bromophenylisothiocyanate and amines is reported. The reaction occurred efficiently in…”
Get full text

Nickel‐Catalysed Decarboxylative Coupling Reactions – An Overview by Arunkumar, T. K., Pallavi, Mohan, Philip, Rose Mary, Anilkumar, Gopinathan

“…Decarboxylative cross‐coupling is a significant method in organic synthesis where inexpensive and stable carboxylic acids are used as substrates for the…”
Get full text