Year |
Citation |
Score |
2021 |
Rajamanickam S, Saraswat M, Venkataramani S, Patel BK. Intermolecular CDC amination of remote and proximal unactivated C -H bonds through intrinsic substrate reactivity - expanding towards a traceless directing group. Chemical Science. 12: 15318-15328. PMID 34976352 DOI: 10.1039/d1sc04365j |
0.733 |
|
2020 |
Rajamanickam S, Sah C, Mir BA, Ghosh S, Sethi G, Yadav V, Venkataramani S, Patel BK. Bu4NI Catalyzed Radical Induced Regioselective N-Alkylations and Arylations of Tetrazoles Using Organic Peroxides/Peresters. The Journal of Organic Chemistry. PMID 31910339 DOI: 10.1021/Acs.Joc.9B02875 |
0.68 |
|
2020 |
Rajamanickam S. Bu4NI Catalyzed Radical Induced Regioselective N-Alkylations and Arylations of Tetrazoles Using Organic Peroxides/Peresters The Journal of Organic Chemistry. 85: 2118-2141. DOI: 10.1021/acs.joc.9b02875 |
0.354 |
|
2020 |
Rajamanickam S. Copper (I) Catalyzed Differential Peroxidation of Terminal and Internal Alkenes Using TBHP European Journal of Organic Chemistry. 252-261. DOI: 10.1002/Ejoc.201901689 |
0.351 |
|
2016 |
Majji G, Rout SK, Rajamanickam S, Guin S, Patel BK. Synthesis of esters via sp(3) C-H functionalisation. Organic & Biomolecular Chemistry. PMID 27488288 DOI: 10.1039/C6Ob01250G |
0.723 |
|
2016 |
Santra SK, Banerjee A, Rajamanickam S, Khatun N, Patel BK. Pd(II)/CuBr2 catalysed keto α-Csp3-H benzoxylation of N,N-dialkylamides directed by o-hydroxy groups. Chemical Communications (Cambridge, England). PMID 26931492 DOI: 10.1039/C6Cc00971A |
0.627 |
|
2016 |
Rajamanickam S. Synthesis of Esters Via sp 3 C–H Functionalisation Organic & Biomolecular Chemistry. 14: 8178-8211. DOI: 10.1039/C6OB01250G |
0.309 |
|
2016 |
Rajamanickam S. Synthesis of 2-amino-substituted-1, 3, 4-thiadiazoles via 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone (DDQ) mediated intramolecular C–S bond formation in thiosemicarbazones Tetrahedron Letters. 57: 1044-1047. DOI: 10.1016/j.tetlet.2016.01.083 |
0.371 |
|
2016 |
Singh SJ, Rajamanickam S, Gogoi A, Patel BK. Synthesis of 2-amino-substituted-1,3,4-thiadiazoles via 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) mediated intramolecular C-S bond formation in thiosemicarbazones Tetrahedron Letters. 57: 1044-1047. DOI: 10.1016/J.Tetlet.2016.01.083 |
0.672 |
|
2016 |
Majji G, Rout SK, Rajamanickam S, Guin S, Patel BK. ChemInform Abstract: Synthesis of Esters via sp3C-H Functionalization Cheminform. 47. DOI: 10.1002/CHIN.201644207 |
0.704 |
|
2016 |
Singh SJ, Rajamanickam S, Gogoi A, Patel BK. ChemInform Abstract: Synthesis of 2-Amino-substituted-1,3,4-thiadiazoles via 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) Mediated Intramolecular C-S Bond Formation in Thiosemicarbazones. Cheminform. 47. DOI: 10.1002/CHIN.201626157 |
0.623 |
|
2016 |
Rajamanickam S. Iron (III)‐Catalyzed Peroxide‐Mediated C‐3 Functionalization of Flavones Advanced Synthesis & Catalysis. 358: 3471-3476. DOI: 10.1002/Adsc.201600565 |
0.477 |
|
2015 |
Rajamanickam S, Majji G, Santra SK, Patel BK. Bu4NI Catalyzed C-N Bond Formation via Cross-Dehydrogenative Coupling of Aryl Ethers (Csp3-H) and Tetrazoles (N-H). Organic Letters. PMID 26528788 DOI: 10.1021/Acs.Orglett.5B02749 |
0.702 |
|
2015 |
Gogoi A, Guin S, Rajamanickam S, Rout SK, Patel BK. Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C-N Bond Over C-S Bond Formation. The Journal of Organic Chemistry. 80: 9016-27. PMID 26332253 DOI: 10.1021/Acs.Joc.5B00956 |
0.716 |
|
2015 |
Majji G, Rajamanickam S, Khatun N, Santra SK, Patel BK. Generation of bis-acyl ketals from esters and benzyl amines under oxidative conditions. The Journal of Organic Chemistry. 80: 3440-6. PMID 25761246 DOI: 10.1021/Jo502903D |
0.661 |
|
2015 |
Rajamanickam S. Bu4NI Catalyzed C–N Bond Formation via Cross-Dehydrogenative Coupling of Aryl Ethers (Csp3–H) and Tetrazoles (N–H) Organic Letter. 17: 5586-5589. DOI: 10.1021/acs.orglett.5b02749 |
0.318 |
|
2015 |
Rajamanickam S. Synthesis of 1, 2, 4-Triazoles via Oxidative Heterocyclization: Selective C–N Bond Over C–S Bond Formation The Journal of Organic Chemistry. 80: 9016-9027. DOI: 10.1021/acs.joc.5b00956 |
0.354 |
|
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