| Year |
Citation |
Score |
| 2022 |
Rhlee JH, Maiti S, Lee JW, Lee HS, Bakhtiyorzoda IA, Lee S, Park J, Kang SJ, Kim YS, Seo JK, Myung K, Choe W, Hong SY. Synthesis of α,β-unsaturated ketones through nickel-catalysed aldehyde-free hydroacylation of alkynes. Communications Chemistry. 5: 13. PMID 36697817 DOI: 10.1038/s42004-022-00633-3 |
0.544 |
|
| 2020 |
Bal A, Maiti S, Mal P. Control of Exothermic Hypervalent Iodine - Primary Amine Reactions. Chemistry, An Asian Journal. PMID 32020772 DOI: 10.1002/Asia.201901683 |
0.624 |
|
| 2020 |
Bal A, Maiti S, Mal P. Intermolecular C‐Arylation of 2‐Amidobiphenyls Overcoming Intramolecular N‐Arylation Asian Journal of Organic Chemistry. 9: 1783-1786. DOI: 10.1002/Ajoc.202000439 |
0.617 |
|
| 2019 |
Maiti S, Kim J, Park JH, Nam D, Lee JB, Kim YJ, Kee JM, Seo JK, Myung K, Rohde JU, Choe W, Kwon OH, Hong SY. Chemoselective Trifluoroethylation Reactions of Quinazolinones and Identification of Photostability. The Journal of Organic Chemistry. PMID 31050290 DOI: 10.1021/Acs.Joc.9B00470 |
0.528 |
|
| 2019 |
Bose A, Maiti S, Sau S, Mal P. An intramolecular C(sp)-H imination using PhI-mCPBA. Chemical Communications (Cambridge, England). PMID 30688962 DOI: 10.1039/C8Cc09100E |
0.669 |
|
| 2019 |
Maiti S, Alam MT, Bal A, Mal P. Nitrenium Ions from Amine‐Iodine(III) Combinations Advanced Synthesis & Catalysis. 361: 4401-4425. DOI: 10.1002/Adsc.201900441 |
0.565 |
|
| 2019 |
Choudhuri K, Maiti S, Mal P. Iodine(III) Enabled Dehydrogenative Aryl C−S Coupling by in situ Generated Sulfenium Ion Advanced Synthesis & Catalysis. 361: 1092-1101. DOI: 10.1002/Adsc.201801510 |
0.601 |
|
| 2018 |
Alam MT, Maiti S, Mal P. The mechanochemical synthesis of quinazolin-4(3)-ones by controlling the reactivity of IBX. Beilstein Journal of Organic Chemistry. 14: 2396-2403. PMID 30254705 DOI: 10.3762/Bjoc.14.216 |
0.642 |
|
| 2018 |
Bal A, Maiti S, Mal P. Iodine(III) Enabled Distal C-H Functionalization of Biarylsulfonanilides. The Journal of Organic Chemistry. PMID 30129758 DOI: 10.1021/Acs.Joc.8B01857 |
0.717 |
|
| 2018 |
Maiti S, Bose A, Mal P. Oxidative N-Arylation for Carbazole Synthesis by C-C Bond Activation. The Journal of Organic Chemistry. PMID 29847942 DOI: 10.1021/Acs.Joc.8B00921 |
0.682 |
|
| 2018 |
Maiti S, Mal P. Soft-Hard Acid/Base-Controlled, Oxidative, N-Selective Arylation of Sulfonanilides via a Nitrenium Ion. The Journal of Organic Chemistry. PMID 29304547 DOI: 10.1021/Acs.Joc.7B02841 |
0.671 |
|
| 2018 |
Alam MT, Maiti S, Mal P. An Intramolecular C(sp2
)-H Amidation Using N
-Iodosuccinimide European Journal of Organic Chemistry. 2018: 4178-4186. DOI: 10.1002/Ejoc.201800688 |
0.652 |
|
| 2018 |
Maiti S, Alam T, Mal P. Soft-Hard Acid-Base-Controlled C−H Trifluoroethoxylation and Trideuteriomethoxylation of Anilides Asian Journal of Organic Chemistry. 7: 715-719. DOI: 10.1002/Ajoc.201800069 |
0.544 |
|
| 2017 |
Maiti S, Mal P. Dehydrogenative Aromatic Ring Fusion for Carbazole Synthesis via C-C/C-N Bond Formation and Alkyl Migration. Organic Letters. PMID 28430447 DOI: 10.1021/Acs.Orglett.7B01117 |
0.687 |
|
| 2017 |
Maiti S, Achar TK, Mal P. An Organic Intermolecular Dehydrogenative Annulation Reaction. Organic Letters. PMID 28406305 DOI: 10.1021/Acs.Orglett.7B00562 |
0.74 |
|
| 2016 |
Achar TK, Maiti S, Mal P. PIDA-I2 mediated direct vicinal difunctionalization of olefins: iodoazidation, iodoetherification and iodoacyloxylation. Organic & Biomolecular Chemistry. PMID 27108786 DOI: 10.1039/C6Ob00532B |
0.687 |
|
| 2015 |
Maiti S, Mal P. Phenyliodine diacetate-mediated intramolecular C(sp2)-H amidation for 1,2-disubstituted benzimidazole synthesis under metal-free conditions Advanced Synthesis and Catalysis. 357: 1416-1424. DOI: 10.1002/Adsc.201401110 |
0.677 |
|
| 2014 |
Maiti S, Mal P. Electron-rich aromatics under ball milling: Oxidative aryl-iodination using I2-oxone and biarylation with I2 Synthetic Communications. 44: 3461-3469. DOI: 10.1080/00397911.2014.946995 |
0.639 |
|
| 2014 |
Achar TK, Maiti S, Mal P. IBX works efficiently under solvent free conditions in ball milling Rsc Adv.. 4: 12834-12839. DOI: 10.1039/C4Ra00415A |
0.685 |
|
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