| Year |
Citation |
Score |
| 2023 |
Maity S, Lopez MA, Bates DM, Lin S, Krska SW, Stahl SS. Polar Heterobenzylic C(sp)-H Chlorination Pathway Enabling Efficient Diversification of Aromatic Nitrogen Heterocycles. Journal of the American Chemical Society. PMID 37642292 DOI: 10.1021/jacs.3c05822 |
0.557 |
|
| 2021 |
Paul N, Maity S, Panja S, Maiti D. Recent Advances in the Nitration of Olefins. Chemical Record (New York, N.Y.). PMID 34569706 DOI: 10.1002/tcr.202100217 |
0.571 |
|
| 2019 |
Maity S, Potter TJ, Ellman JA. α-Branched amines by catalytic 1,1-addition of C-H bonds and aminating agents to terminal alkenes. Nature Catalysis. 2: 756-762. PMID 32879907 DOI: 10.1038/s41929-019-0330-7 |
0.818 |
|
| 2019 |
Baccalini A, Vergura S, Dolui P, Maiti S, Dutta S, Maity S, Khan FF, Lahiri GK, Zanoni G, Maiti D. Cobalt-Catalyzed C(sp)-H Allylation of Biphenyl Amines with Unbiased Terminal Olefins. Organic Letters. PMID 31638402 DOI: 10.1021/Acs.Orglett.9B03484 |
0.678 |
|
| 2019 |
Agasti S, Maiti S, Maity S, Anniyappan M, Talawar M, Maiti D. Bismuth nitrate as a source of nitro radical in ipso-nitration of carboxylic acids Polyhedron. 172: 120-124. DOI: 10.1016/J.Poly.2019.04.005 |
0.738 |
|
| 2018 |
Boerth JA, Maity S, Williams SK, Mercado BQ, Ellman JA. Selective and synergistic cobalt(III)-catalyzed three-component C-H bond addition to dienes and aldehydes. Nature Catalysis. 1: 673-679. PMID 30221249 DOI: 10.1038/s41929-018-0123-4 |
0.814 |
|
| 2017 |
Thrimurtulu N, Khan S, Maity S, Volla CMR, Maiti D. Palladium catalyzed direct aliphatic γC(sp(3))-H alkenylation with alkenes and alkenyl iodides. Chemical Communications (Cambridge, England). PMID 29104971 DOI: 10.1039/C7Cc05703B |
0.639 |
|
| 2017 |
Maity S, Dolui P, Kancherla R, Maiti D. Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction. Chemical Science. 8: 5181-5185. PMID 28970904 DOI: 10.1039/C7Sc01204G |
0.795 |
|
| 2017 |
Gholap AVA, Maity S, Schulzke C, Maiti D, Kapdi AR. Synthesis of Cu-catalysed quinazolinones using a Csp3-H functionalisation/cyclisation strategy. Organic & Biomolecular Chemistry. PMID 28805837 DOI: 10.1039/C7Ob01723E |
0.623 |
|
| 2016 |
Maity S, Hoque E, Dhawa U, Maiti D. Palladium catalyzed selective distal C-H olefination of biaryl systems. Chemical Communications (Cambridge, England). PMID 27853761 DOI: 10.1039/C6Cc07861C |
0.628 |
|
| 2016 |
Dey A, Maity S, Maiti D. Reaching the south: metal-catalyzed transformation of the aromatic para-position. Chemical Communications (Cambridge, England). PMID 27559937 DOI: 10.1039/C6Cc05235E |
0.594 |
|
| 2016 |
Maity S, Kancherla R, Dhawa U, Hoque E, Pimparkar S, Maiti D. Switch to Allylic Selectivity in Cobalt-Catalyzed Dehydrogenative Heck Reactions with Unbiased Aliphatic Olefins Acs Catalysis. 6: 5493-5499. DOI: 10.1021/Acscatal.6B01816 |
0.798 |
|
| 2015 |
Bag S, Patra T, Modak A, Deb A, Maity S, Dutta U, Dey A, Kancherla R, Maji A, Hazra A, Bera M, Maiti D. Remote para-C-H Functionalization of Arenes by a D-Shaped Biphenyl Template-Based Assembly. Journal of the American Chemical Society. 137: 11888-91. PMID 26361337 DOI: 10.1021/Jacs.5B06793 |
0.685 |
|
| 2015 |
Agasti S, Maity S, Szabo KJ, Maiti D. Palladium-Catalyzed Synthesis of 2,3-Disubstituted Benzofurans: An Approach Towards the Synthesis of Deuterium Labeled Compounds. Advanced Synthesis & Catalysis. 357: 2331-2338. PMID 26347405 DOI: 10.1002/Adsc.201500308 |
0.778 |
|
| 2015 |
Maity S, Agasti S, Earsad AM, Hazra A, Maiti D. Nickel-Catalyzed Insertion of Alkynes and Electron-Deficient Olefins into Unactivated sp(3) CH Bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 11320-4. PMID 26121618 DOI: 10.1002/Chem.201501962 |
0.777 |
|
| 2014 |
Dutta U, Maity S, Kancherla R, Maiti D. Aerobic oxynitration of alkynes with (t)BuONO and TEMPO. Organic Letters. 16: 6302-5. PMID 25401303 DOI: 10.1021/Ol503025N |
0.792 |
|
| 2014 |
Modak A, Dutta U, Kancherla R, Maity S, Bhadra M, Mobin SM, Maiti D. Predictably selective (sp3)C-O bond formation through copper catalyzed dehydrogenative coupling: facile synthesis of dihydro-oxazinone derivatives. Organic Letters. 16: 2602-5. PMID 24761793 DOI: 10.1021/Ol500670H |
0.757 |
|
| 2014 |
Snieckus V, Kim J, Modak A, Dutta U, Kancherla R, Maity S, Bhadra M, Mobin SM, Maiti D. Dihydro-oxazinones from Salicylamides Synfacts. 10: 683-683. DOI: 10.1055/S-0034-1378255 |
0.749 |
|
| 2014 |
Maity S, Naveen T, Sharma U, Maiti D. Efficient and stereoselective nitration of olefins with AgNO2 and TEMPO Synlett. 25: 603-607. DOI: 10.1055/S-0033-1340467 |
0.813 |
|
| 2013 |
Deb A, Manna S, Modak A, Patra T, Maity S, Maiti D. Oxidative trifluoromethylation of unactivated olefins: an efficient and practical synthesis of α-trifluoromethyl-substituted ketones. Angewandte Chemie (International Ed. in English). 52: 9747-50. PMID 23934929 DOI: 10.1002/Anie.201303576 |
0.768 |
|
| 2013 |
Maity S, Naveen T, Sharma U, Maiti D. Stereoselective nitration of olefins with (t)BuONO and TEMPO: direct access to nitroolefins under metal-free conditions. Organic Letters. 15: 3384-7. PMID 23772945 DOI: 10.1021/Ol401426P |
0.793 |
|
| 2013 |
Naveen T, Maity S, Sharma U, Maiti D. A predictably selective nitration of olefin with Fe(NO3)3 and TEMPO. The Journal of Organic Chemistry. 78: 5949-54. PMID 23692506 DOI: 10.1021/Jo400598P |
0.799 |
|
| 2013 |
Maity S, Manna S, Rana S, Naveen T, Mallick A, Maiti D. Efficient and stereoselective nitration of mono- and disubstituted olefins with AgNO2 and TEMPO. Journal of the American Chemical Society. 135: 3355-8. PMID 23406020 DOI: 10.1021/Ja311942E |
0.8 |
|
| 2012 |
Modak A, Deb A, Patra T, Rana S, Maity S, Maiti D. A general and efficient aldehyde decarbonylation reaction by using a palladium catalyst. Chemical Communications (Cambridge, England). 48: 4253-5. PMID 22441208 DOI: 10.1039/C2Cc31144E |
0.76 |
|
| 2012 |
Manna S, Maity S, Rana S, Agasti S, Maiti D. ipso-Nitration of arylboronic acids with bismuth nitrate and perdisulfate. Organic Letters. 14: 1736-9. PMID 22409632 DOI: 10.1021/Ol300325T |
0.79 |
|
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