Reddi RN - Search Results

1

Computational Screening of the Natural Product Osthole and Its Derivates for Anti-Inflammatory Activity.

Mosebarger A, Reddi RN, Menon R, Kammala AK. Mosebarger A, et al. Among authors: reddi rn. Life (Basel). 2022 Mar 30;12(4):505. doi: 10.3390/life12040505. Life (Basel). 2022. PMID: 35454996 Free PMC article.

2

Tunable Methacrylamides for Covalent Ligand Directed Release Chemistry.

Reddi RN, Resnick E, Rogel A, Rao BV, Gabizon R, Goldenberg K, Gurwicz N, Zaidman D, Plotnikov A, Barr H, Shulman Z, London N. Reddi RN, et al. J Am Chem Soc. 2021 Apr 7;143(13):4979-4992. doi: 10.1021/jacs.0c10644. Epub 2021 Mar 24. J Am Chem Soc. 2021. PMID: 33761747 Free PMC article.

3

Site-Specific Labeling of Endogenous Proteins Using CoLDR Chemistry.

Reddi RN, Rogel A, Resnick E, Gabizon R, Prasad PK, Gurwicz N, Barr H, Shulman Z, London N. Reddi RN, et al. J Am Chem Soc. 2021 Dec 8;143(48):20095-20108. doi: 10.1021/jacs.1c06167. Epub 2021 Nov 24. J Am Chem Soc. 2021. PMID: 34817989 Free PMC article.

4

Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease.

Douangamath A, Fearon D, Gehrtz P, Krojer T, Lukacik P, Owen CD, Resnick E, Strain-Damerell C, Aimon A, Ábrányi-Balogh P, Brandão-Neto J, Carbery A, Davison G, Dias A, Downes TD, Dunnett L, Fairhead M, Firth JD, Jones SP, Keeley A, Keserü GM, Klein HF, Martin MP, Noble MEM, O'Brien P, Powell A, Reddi RN, Skyner R, Snee M, Waring MJ, Wild C, London N, von Delft F, Walsh MA. Douangamath A, et al. Among authors: reddi rn. Nat Commun. 2020 Oct 7;11(1):5047. doi: 10.1038/s41467-020-18709-w. Nat Commun. 2020. PMID: 33028810 Free PMC article.

5

Oxidant controlled regio- and stereodivergent azidohydroxylation of alkenes via I2 catalysis.

Prasad PK, Reddi RN, Sudalai A. Prasad PK, et al. Among authors: reddi rn. Chem Commun (Camb). 2015 Jun 28;51(51):10276-9. doi: 10.1039/c5cc02374b. Chem Commun (Camb). 2015. PMID: 25921612

6

Regioselective Oxo-Amination of Alkenes and Enol Ethers with N-Bromosuccinimide-Dimethyl Sulfoxide Combination: A Facile Synthesis of α-Amino-Ketones and Esters.

Prasad PK, Reddi RN, Sudalai A. Prasad PK, et al. Among authors: reddi rn. Org Lett. 2016 Feb 5;18(3):500-3. doi: 10.1021/acs.orglett.5b03540. Epub 2016 Jan 22. Org Lett. 2016. PMID: 26800214

7

I2-catalyzed regioselective oxo- and hydroxy-acyloxylation of alkenes and enol ethers: a facile access to α-acyloxyketones, esters, and diol derivatives.

Reddi RN, Prasad PK, Sudalai A. Reddi RN, et al. Org Lett. 2014 Nov 7;16(21):5674-7. doi: 10.1021/ol5027393. Epub 2014 Oct 29. Org Lett. 2014. PMID: 25351821

8

Recent methods for the synthesis of α-acyloxy ketones.

Prasad PK, Reddi RN, Arumugam S. Prasad PK, et al. Among authors: reddi rn. Org Biomol Chem. 2018 Dec 12;16(48):9334-9348. doi: 10.1039/c8ob02881h. Org Biomol Chem. 2018. PMID: 30516787 Review.

9

N-Heterocyclic Carbene Catalyzed Oxidative Coupling of Alkenes/α-Bromoacetophenones with Aldehydes: A Facile Entry to α,β-Epoxy Ketones.

Reddi RN, Prasad PK, Sudalai A. Reddi RN, et al. Angew Chem Int Ed Engl. 2015 Nov 16;54(47):14150-3. doi: 10.1002/anie.201507363. Epub 2015 Sep 21. Angew Chem Int Ed Engl. 2015. PMID: 26387970

10

I2-mediated regioselective C-3 azidation of indoles.

Prasad PK, Kalshetti RG, Reddi RN, Kamble SP, Sudalai A. Prasad PK, et al. Among authors: reddi rn. Org Biomol Chem. 2016 Mar 21;14(11):3027-30. doi: 10.1039/c6ob00295a. Epub 2016 Feb 25. Org Biomol Chem. 2016. PMID: 26911555

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