| Year |
Citation |
Score |
| 2024 |
Aich D, Das KK, Panda S. Conversion of Phenols and Anilines to -Olefins via Oxidation, Wittig Olefination, and Stereoselective Olefin Isomerization. Organic Letters. 26: 10791-10796. PMID 39644258 DOI: 10.1021/acs.orglett.4c03789 |
0.82 |
|
| 2024 |
Mahato S, Ghorai D, Das KK, Roy L, Panda S. Alkoxide-Assisted Stereoselective Functionalization of 1,2-Bis-boronic Esters Under Photoredox Catalysis. Organic Letters. PMID 39052950 DOI: 10.1021/acs.orglett.4c02469 |
0.824 |
|
| 2024 |
Das KK, Aich D, Dey S, Panda S. One pot conversion of phenols and anilines to aldehydes and ketones exploiting α gem boryl carbanions. Nature Communications. 15: 3794. PMID 38714666 DOI: 10.1038/s41467-024-47156-0 |
0.838 |
|
| 2024 |
Manna S, Aich D, Hazra S, Khandelwal S, Panda S. Reactivity of 1,3-enyne MIDA boronates: exploration of novel 1,2-alkyne shift -difluorination. Chemical Science. 15: 4989-4995. PMID 38550673 DOI: 10.1039/d3sc06918d |
0.781 |
|
| 2023 |
Paul S, Panda S. Synthesis of Boronic Esters from Organometallic Reagents and Bis(pinacolato)diboron. Chemistry, An Asian Journal. e202300911. PMID 38131458 DOI: 10.1002/asia.202300911 |
0.835 |
|
| 2023 |
Hazra S, Panda S. Stereoselective Synthesis of Silylated Vinylboronates by a Boron-Wittig Reaction and Their Application to Tetrasubstituted Olefins. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303056. PMID 37991686 DOI: 10.1002/chem.202303056 |
0.837 |
|
| 2023 |
Ghorai D, Das KK, Panda S. Carbonyl group directed synthesis of 3-boryl-3-substituted alkenyl oxindoles and tetrasubstituted β-borylenones. Chemical Communications (Cambridge, England). PMID 37982264 DOI: 10.1039/d3cc04788a |
0.783 |
|
| 2023 |
Manna S, Paul S, Kong WY, Aich D, Sahoo R, Tantillo DJ, Panda S. Stereodivergent Zweifel Olefination and its Mechanistic Dichotomy. Angewandte Chemie (International Ed. in English). e202309136. PMID 37495925 DOI: 10.1002/anie.202309136 |
0.763 |
|
| 2023 |
Das KK, Panda S. 1,2-Metallate Rearrangement Using Indole Boronate Species to Access 2,3-Diarylindoles and Indolines. Organic Letters. 25: 314-319. PMID 36602541 DOI: 10.1021/acs.orglett.2c03761 |
0.574 |
|
| 2022 |
Aich D, Kumar P, Ghorai D, Kanti Das K, Panda S. Recent advances in the synthesis and reactivity of MIDA boronates. Chemical Communications (Cambridge, England). PMID 36382511 DOI: 10.1039/d2cc04893k |
0.761 |
|
| 2022 |
Mondal S, Das KK, Panda S. Iron catalysis, a new horizon towards the organoboron-mediated C-C cross-coupling. Chemistry, An Asian Journal. PMID 36219672 DOI: 10.1002/asia.202200836 |
0.462 |
|
| 2022 |
Manna S, Kakumachi S, Das KK, Tsuchiya Y, Adachi C, Panda S. Mechanistic dichotomy in the solvent dependent access to -allylic amines decarboxylative vinylation of amino acids. Chemical Science. 13: 9678-9684. PMID 36091905 DOI: 10.1039/d2sc02090d |
0.673 |
|
| 2022 |
Panda S, Saha A, Chauhan MS, Singla SK. Development of homologous hemizona assay as a potential predictor of fertility in buffalo bulls: A preliminary approach. Reproduction in Domestic Animals = Zuchthygiene. PMID 35862253 DOI: 10.1111/rda.14209 |
0.187 |
|
| 2022 |
Hazra S, Mahato S, Das KK, Panda S. Transition Metal-Free Heterocyclic Carbon-Boron Bond Formation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 35438817 DOI: 10.1002/chem.202200556 |
0.796 |
|
| 2022 |
Das KK, Mahato S, Hazra S, Panda S. Development of Methods to the Synthesis of β-Boryl Acyls, Imines and Nitriles. Chemical Record (New York, N.Y.). e202100290. PMID 35088513 DOI: 10.1002/tcr.202100290 |
0.805 |
|
| 2021 |
Kalra S, Dhamannapatil P, Panda S, Singh S, Sarwalia P, Mohanty AK, Datta TK, Kaushik JK. Recombinant expression and molecular characterization of buffalo sperm lysozyme-like protein 1. Protein Expression and Purification. 190: 105993. PMID 34656738 DOI: 10.1016/j.pep.2021.105993 |
0.209 |
|
| 2021 |
Nandy S, Paul S, Das KK, Kumar P, Ghorai D, Panda S. Synthesis and reactivity of alkynyl boron compounds. Organic & Biomolecular Chemistry. PMID 34374405 DOI: 10.1039/d1ob00465d |
0.796 |
|
| 2021 |
Barman S, Panda S. Body composition and Aerobic capacity among the Volleyball players of the University: An assessment Research Review International Journal of Multidisciplinary. 6: 239-244. DOI: 10.31305/RRIJM.2021.V06.I01.047 |
0.169 |
|
| 2021 |
Ghosh R, Panda S. Women Workers Rights and Gender Equality: A critical analysis Research Review International Journal of Multidisciplinary. 6: 146-153. DOI: 10.31305/RRIJM.2020.V06.I02.024 |
0.17 |
|
| 2021 |
Manna S, Das KK, Aich D, Panda S. Synthesis and Reactivity of Allenylboron Compounds Advanced Synthesis & Catalysis. 363: 2444-2463. DOI: 10.1002/ADSC.202100025 |
0.728 |
|
| 2020 |
Kanti Das K, Manna S, Panda S. Transition metal catalyzed asymmetric multicomponent reactions of unsaturated compounds using organoboron reagents. Chemical Communications (Cambridge, England). PMID 33350405 DOI: 10.1039/d0cc06460b |
0.804 |
|
| 2020 |
Das KK, Paul S, Panda S. Transition metal-free synthesis of alkyl pinacol boronates. Organic & Biomolecular Chemistry. PMID 33146221 DOI: 10.1039/d0ob01721c |
0.835 |
|
| 2020 |
Panda S, Das KK. Functionalization of Heterocycles Through 1,2-Metallate Rearrangement of Boron Ate Complex. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32667713 DOI: 10.1002/chem.202002573 |
0.407 |
|
| 2020 |
Paul S, Das KK, Manna S, Panda S. Frontispiece: Transition‐Metal‐Free Synthesis of Heterobiaryls through 1,2‐Migration of Boronate Complex Chemistry – a European Journal. 26. DOI: 10.1002/chem.202080963 |
0.784 |
|
| 2019 |
Panda S, Paul S, Das KK, Manna S. Transition Metal Free Synthesis of Heterobiaryls Through 1,2-Migration of Boronate Complex. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31738451 DOI: 10.1002/chem.201904761 |
0.83 |
|
| 2018 |
Panda S, Ready JM. Tandem Allylation/1,2-Boronate Rearrangement for the Asymmetric Synthesis of Indolines with Adjacent Quaternary Stereocenters. Journal of the American Chemical Society. PMID 30240211 DOI: 10.1021/jacs.8b06629 |
0.632 |
|
| 2017 |
Panda S, Ready JM. Palladium Catalyzed Asymmetric Three Component Cou-pling of Boronic Esters, Indoles and Allylic Acetates. Journal of the American Chemical Society. PMID 28414430 DOI: 10.1021/jacs.7b01410 |
0.649 |
|
| 2017 |
Panda S. Cultural Juxtaposition in R.K Naryan’s novel The Guide International Journal of English Literature and Social Sciences. 2: 28-31. DOI: 10.24001/IJELS.2.5.4 |
0.187 |
|
| 2016 |
Panda S. How the Developmental Programmes Breakdown among the Marginalised Tribal Community: A Case of Lodhas in West Bengal Asian Man (the) - An International Journal. 10: 111. DOI: 10.5958/0975-6884.2016.00015.3 |
0.176 |
|
| 2015 |
Panda S, Coffin A, Nguyen QN, Tantillo DJ, Ready JM. Synthesis and Utility of Dihydropyridine Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 26694785 DOI: 10.1002/Anie.201510027 |
0.699 |
|
| 2015 |
Panda S, Bisht S, Malakar D, Mohanty AK, Kaushik JK. In vitro culture of functionally active buffalo hepatocytes isolated by using a simplified manual perfusion method. Plos One. 10: e0118841. PMID 25790478 DOI: 10.1371/journal.pone.0118841 |
0.246 |
|
| 2014 |
Gadave KS, Panda S, Singh S, Kalra S, Malakar D, Mohanty AK, Kaushik JK. Structural and functional insights into the catalytic inactivity of the major fraction of buffalo milk xanthine oxidoreductase. Plos One. 9: e87618. PMID 24498153 DOI: 10.1371/journal.pone.0087618 |
0.272 |
|
| 2013 |
Pearson AJ, Panda S, Bunge SD. Synthesis of a potential intermediate for TMC-95A via an organocatalyzed aldol reaction. The Journal of Organic Chemistry. 78: 9921-8. PMID 24024913 DOI: 10.1021/Jo4017315 |
0.557 |
|
| 2011 |
Pearson AJ, Panda S. N-Prolinylanthranilamide pseudopeptides as bifunctional organocatalysts for asymmetric aldol reactions. Organic Letters. 13: 5548-51. PMID 21958056 DOI: 10.1021/Ol202284N |
0.564 |
|
| 2011 |
Pearson AJ, Panda S. N-Prolinylanthranilic acid derivatives as bifunctional organocatalysts for asymmetric aldol reactions Tetrahedron. 67: 3969-3975. DOI: 10.1016/J.Tet.2011.04.033 |
0.535 |
|
| 2011 |
Pearson AJ, Panda S. ChemInform Abstract: N-Prolinylanthranilic Acid Derivatives as Bifunctional Organocatalysts for Asymmetric Aldol Reactions. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201141059 |
0.428 |
|
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