Year |
Citation |
Score |
2018 |
Prasad PK, Reddi RN, Arumugam S. Recent methods for the synthesis of α-acyloxy ketones. Organic & Biomolecular Chemistry. PMID 30516787 DOI: 10.1039/c8ob02881h |
0.614 |
|
2017 |
Wu X, Hao L, Zhang Y, Rakesh M, Reddi RN, Yang S, Song BA, Chi YR. Construction of Fused Pyrrolidines and β-Lactones by Carbene-Catalyzed C-N, C-C, and C-O Bond Formations. Angewandte Chemie (International Ed. in English). PMID 28295941 DOI: 10.1002/anie.201700045 |
0.599 |
|
2017 |
Wu X, Zhang Y, Wang Y, Ke J, Jeret M, Reddi RN, Yang S, Song BA, Chi YR. Polyhalides as Efficient and Mild Oxidants for Oxidative Carbene Organocatalysis by Radical Processes. Angewandte Chemie (International Ed. in English). PMID 28151571 DOI: 10.1002/anie.201611692 |
0.576 |
|
2016 |
Prasad PK, Kalshetti RG, Reddi RN, Kamble SP, Sudalai A. I2-mediated regioselective C-3 azidation of indoles. Organic & Biomolecular Chemistry. 14: 3027-30. PMID 26911555 DOI: 10.1039/C6Ob00295A |
0.554 |
|
2016 |
Prasad PK, Reddi RN, Sudalai A. Regioselective Oxo-Amination of Alkenes and Enol Ethers with N-Bromosuccinimide-Dimethyl Sulfoxide Combination: A Facile Synthesis of α-Amino-Ketones and Esters. Organic Letters. 18: 500-3. PMID 26800214 DOI: 10.1021/Acs.Orglett.5B03540 |
0.641 |
|
2015 |
Reddi RN, Prasad PK, Sudalai A. N-Heterocyclic Carbene Catalyzed Oxidative Coupling of Alkenes/α-Bromoacetophenones with Aldehydes: A Facile Entry to α,β-Epoxy Ketones. Angewandte Chemie (International Ed. in English). 54: 14150-3. PMID 26387970 DOI: 10.1002/Anie.201507363 |
0.656 |
|
2014 |
Reddi RN, Prasad PK, Sudalai A. I2-catalyzed regioselective oxo- and hydroxy-acyloxylation of alkenes and enol ethers: a facile access to α-acyloxyketones, esters, and diol derivatives. Organic Letters. 16: 5674-7. PMID 25351821 DOI: 10.1021/Ol5027393 |
0.646 |
|
2013 |
Reddi RN, Malekar PV, Sudalai A. N-heterocyclic carbene catalyzed regioselective oxo-acyloxylation of alkenes with aromatic aldehydes: a high yield synthesis of α-acyloxy ketones and esters. Organic & Biomolecular Chemistry. 11: 6477-82. PMID 23969565 DOI: 10.1039/C3Ob41551A |
0.687 |
|
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