Pradeep Panyam

Pradeep Panyam
  • PhD
  • PostDoc Position at University of Stuttgart

About

11
Publications
1,270
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137
Citations
Current institution
University of Stuttgart
Current position
  • PostDoc Position

Publications

Publications (11)
Article
Non‐porous polyurethane‐based monoliths were prepared under solvent‐induced phase separation conditions. They possess low specific surface areas of 0.15 m2/g, pore volumes of 1 μL/g and a non‐permanent, solvent‐induced microporosity with pore dimensions ≤ 1 nm. Mesoporosity can be introduced by varying the monomers and solvents. A tuning of the ave...
Article
Full-text available
Ketones are the key functional group that recurs in chemistry and biology, and accessing them through simple and economic ways is highly desirable. Herein, we report the synthesis of unsymmetrical ketones from abundant toluene and alkyl esters, where volatile alcohols are the sole byproduct. This protocol applies to a repertoire of substrates beari...
Article
Polymeric mesoporous monoliths were prepared via ring-opening metathesis polymerization (ROMP) from norbornene (NBE), 1,4,4a,5,8,8a-hexahydro-1,4,5,8-exo,endo-dimethanonaphthalene (DMN-H6), tris(norborn-2-enylmethylenoxy)methylsilane and the 1st-generation Grubbs catalyst [RuCl2(PCy3)2(CHC6H5)] in the presence of 2-propanol and toluene and...
Article
Full-text available
Rh(I) NHC and Rh(III) Cp* NHC complexes (Cp*=pentamethylcyclopentadienyl, NHC=N‐heterocyclic carbene=pyrid‐2‐ylimidazol‐2‐ylidene (Py−Im), thiophen‐2‐ylimidazol‐2‐ylidene) are presented. Selected catalysts were selectively immobilized inside the mesopores of SBA‐15 with average pore diameters of 5.0 and 6.2 nm. Together with their homogenous progen...
Chapter
The chemistry of both low- and high-oxidation state vanadium, niobium, tantalum, chromium, molybdenum and tungsten N-heterocyclic carbene (NHC) and mesoionic carbene complexes is outlined. This article mostly focuses on their synthesis, relevant structural aspects and peculiarities, but also addresses some applications and use of these complexes, e...
Article
Full-text available
Reaction of CrCl2(N‐tBu)2 with 1,3‐dimethylimidazol‐2‐ylidene (IMe), 1,3‐dimethyl‐4,5‐dichloroimidazol‐2‐ylidene (IMeCl2), 1,3‐di(2‐propyl)imidazol‐2‐ylidene (IPr), 1,3‐dimesitylimidazol‐2‐ylidene (IMes) and 1,3‐bis(2,6‐(2‐Pr)2C6H3)imidazol‐2‐ylidene (IDipp) yields the corresponding N‐heterocyclic carbene (NHC) adducts CrCl2(IMe)(N‐tBu)2 (1), CrCl2...
Article
Predominantly, aggressive acid chlorides and stoichiometric coupling reagents are employed in the acylating process for synthesizing carbonyl tethered heterocycles. Herein, we report simple acyl sources, viz. methyl and phenyl esters which acylate oxindoles via mixed Claisen condensation. This straightforward protocol is mediated by LiHMDS and KOtB...
Article
Rationally designed fluorene-based mono- and bimetallic Pd-PEPPSI complexes were synthesized and demonstrated to be effective for the one-pot sequential α-arylation/alkylation of oxindoles. This streamlined approach offers efficient access to functionalized 3,3-disubstituted oxindoles in excellent yields (up to 89%) under mild reaction conditions.
Article
Topologically constrained naphthalimide appended Pd-NHCs were synthesized and characterized. These structurally related complexes were catalytically compared with the previously synthesized Pd-NHC in the regioselective heteroannulation of o-haloanilines and arylethynyl-trimethylsilane. The unique effect of the additive on the product selectivity ha...
Article
Monometallic and bimetallic palladium(II)/N‐heterocyclic carbene complexes appended with naphthalimide or bisnaphthalimide moieties were designed, synthesized, and characterized. Employment of these catalysts brings about the step‐economic and regioselective heteroannulation of tertiary propargyl alcohols with o ‐haloanilines resulting in biologica...
Article
Palladium-catalyzed synthetic methodology has been developed for the synthesis of 2-aminobenzenesulfonic acids from benzothiazoles in good to excellent yields using chloramine-B in alkaline (pH 12) acetonitrile/water (1:1) at 80 °C.

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