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Siva Sankar Murthy Bandaru

Explore the profile of Siva Sankar Murthy Bandaru including associated specialties, affiliations and a list of published articles. Areas
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Articles 11
Citations 33
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Recent Articles
1.
Napierkowski M, Schone T, Bandaru S, Judernatz J, Schulig L, Schmidt L, et al.
ChemMedChem . 2024 Nov; 20(5):e202400727. PMID: 39526984
The biological properties of pentathiepins have been intensively studied in recent years. Although the proposed mechanism of action requires activation by intracellular thiols, the dependence of activity on the stability...
2.
Malhotra V, Elvers B, Dolai R, Chrysochos N, Bandaru S, Gangber T, et al.
J Am Chem Soc . 2024 Oct; 146(43):29481-29490. PMID: 39425654
Herein, we report nickel(0)-catalyzed cross-coupling reactions of NHC/CAAC-based carbodicarbene (NHC = -heterocyclic carbene and CAAC = cyclic(alkyl)(amino)carbene) with different aryl chlorides, bromides, and iodides. The resulting aryl-substituted cationic carbodicarbene derivatives...
3.
Wolff L, Bandaru S, Eger E, Lam H, Napierkowski M, Baecker D, et al.
Int J Mol Sci . 2021 Jul; 22(14). PMID: 34299253
Pentathiepins are polysulfur-containing compounds that exert antiproliferative and cytotoxic activity in cancer cells, induce oxidative stress and apoptosis, and inhibit glutathione peroxidase (GPx1). This renders them promising candidates for anticancer...
4.
Bandaru S, Bhilare S, Schulzke C, Kapdi A
Chem Rec . 2020 Nov; 21(1):188-203. PMID: 33231365
Phosphines have, in combination with transition metals, played a pivotal role in the rapid development of efficient catalytic processes. Caged phosphines constitute a class of three-dimensional scaffolds providing unique control...
5.
Behnisch-Cornwell S, Bandaru S, Napierkowski M, Wolff L, Zubair M, Urbainsky C, et al.
ChemMedChem . 2020 Apr; 15(16):1515-1528. PMID: 32311219
A novel class of glutathione peroxidase 1 (GPx1) inhibitors, namely tri- and tetracyclic pentathiepins, has been identified that is approximately 15 times more potent than the most active known GPx1...
6.
Bandaru S, Bhilare S, Cardozo J, Chrysochos N, Schulzke C, Sanghvi Y, et al.
J Org Chem . 2019 Jun; 84(14):8921-8940. PMID: 31181881
The thioetherification of heteroaryl chlorides is an essential synthetic methodology that provides access to bioactive drugs and agrochemicals. Due to their (actual or potential) industrial importance, the development of efficient...
7.
Bhilare S, Bandaru S, Shah J, Chrysochos N, Schulzke C, Sanghvi Y, et al.
J Org Chem . 2018 Oct; 83(21):13088-13102. PMID: 30296085
A mild, general, and highly efficient catalytic etherification protocol for chloroheteroarenes was developed using the Pd/PTABS catalytic system. The protocol is selective for the etherification of chloroheteroarenes using a large...
8.
Bhilare S, Bandaru S, Kapdi A, Sanghvi Y, Schulzke C
Curr Protoc Nucleic Acid Chem . 2018 Aug; 74(1):e58. PMID: 30129702
The synthesis and catalytic applications of the highly water-soluble ligand 7-phospha-1,3,5-triaza-admantane butane sultonate (PTABS) has been described. The synthesized PTABS ligand along with palladium acetate exhibits excellent reactivity towards the...
9.
Bandaru S, Dzubiel D, Ihmels H, Karbasiyoun M, Mahmoud M, Schulzke C
Beilstein J Org Chem . 2018 Aug; 14:1871-1884. PMID: 30112092
9-Arylbenzo[]quinolizinium derivatives were prepared with base-free Suzuki-Miyaura coupling reactions between benzo[]quinolizinium-9-trifluoroborate and selected benzenediazonium salts. In addition, the Sonogashira coupling reaction between 9-iodobenzo[]quinolizinium and the arylalkyne derivatives yielded four novel...
10.
Bandaru S, Kapdi A, Schulzke C
Acta Crystallogr E Crystallogr Commun . 2018 Jun; 74(Pt 2):137-140. PMID: 29850040
The mol-ecular structure of the title compound, CHNO, is nearly planar despite the chair conformation of the morpholine moiety. In the crystal, the mol-ecules form sheets parallel to the axis,...