Year |
Citation |
Score |
2019 |
Kaur R, Thakur NS, Chandna S, Bhaumik J. Development of agri-biomass based lignin derived zinc oxide nanocomposites as promising UV protectant-cum-antimicrobial agents. Journal of Materials Chemistry. B. PMID 31799593 DOI: 10.1039/C9Tb01569H |
0.336 |
|
2017 |
Thakur NS, Bhaumik J, Kirar S, Banerjee UC. Development of Gold-Based Phototheranostic Nanoagents through a Bioinspired Route and Their Applications in Photodynamic Therapy Acs Sustainable Chemistry & Engineering. 5: 7950-7960. DOI: 10.1021/Acssuschemeng.7B01501 |
0.34 |
|
2016 |
Ghosh S, Bhaumik J, Banoth L, Banesh S, Banerjee UC. Chemoenzymatic Route for the Synthesis of (S)-Moprolol, a Potential β-Blocker. Chirality. PMID 26821612 DOI: 10.1002/Chir.22574 |
0.318 |
|
2016 |
Bhaumik J, Gogia G, Kirar S, Vijay L, Thakur NS, Banerjee UC, Laha JK. Bioinspired nanophotosensitizers: Synthesis and characterization of porphyrin-noble metal nanoparticle conjugates New Journal of Chemistry. 40: 724-731. DOI: 10.1039/C5Nj02056E |
0.355 |
|
2015 |
Bhaumik J, Thakur NS, Aili PK, Ghanghoriya A, Mittal AK, Banerjee UC. Bioinspired Nanotheranostic Agents: Synthesis, Surface Functionalization, and Antioxidant Potential. Acs Biomaterials Science & Engineering. 1: 382-392. PMID 33445243 DOI: 10.1021/Ab500171A |
0.322 |
|
2014 |
Liu M, Ptaszek M, Mass O, Minkler DF, Sommer RD, Bhaumik J, Lindsey JS. Regioselective β-pyrrolic electrophilic substitution of hydrodipyrrin-dialkylboron complexes facilitates access to synthetic models for chlorophyll f New Journal of Chemistry. 38: 1717-1730. DOI: 10.1039/C3Nj01508D |
0.651 |
|
2009 |
McCarthy JR, Bhaumik J, Merbouh N, Weissleder R. High-yielding syntheses of hydrophilic conjugatable chlorins and bacteriochlorins. Organic & Biomolecular Chemistry. 7: 3430-6. PMID 19675897 DOI: 10.1039/B908713C |
0.374 |
|
2009 |
Bhaumik J, Weissleder R, McCarthy JR. Synthesis and photophysical properties of sulfonamidophenyl porphyrins as models for activatable photosensitizers. The Journal of Organic Chemistry. 74: 5894-901. PMID 19610602 DOI: 10.1021/Jo900832Y |
0.367 |
|
2009 |
Mroz P, Bhaumik J, Dogutan DK, Aly Z, Kamal Z, Khalid L, Kee HL, Bocian DF, Holten D, Lindsey JS, Hamblin MR. Imidazole metalloporphyrins as photosensitizers for photodynamic therapy: Role of molecular charge, central metal and hydroxyl radical production Cancer Letters. 282: 63-76. PMID 19346065 DOI: 10.1016/J.Canlet.2009.02.054 |
0.639 |
|
2008 |
Kee HL, Bhaumik J, Diers JR, Mroz P, Hamblin MR, Bocian DF, Lindsey JS, Holten D. Photophysical Characterization of Imidazolium-Substituted Pd(II), In(III), and Zn(II) Porphyrins as Photosensitizers for Photodynamic Therapy. Journal of Photochemistry and Photobiology. a, Chemistry. 200: 346-355. PMID 20016663 DOI: 10.1016/J.Jphotochem.2008.08.006 |
0.546 |
|
2008 |
Kee HL, Bhaumik J, Diers JR, Mroz P, Hamblin MR, Bocian DF, Lindsey JS, Holten D. Photophysical characterization of imidazolium-substituted Pd(II), In(III), and Zn(II) porphyrins as photosensitizers for photodynamic therapy Journal of Photochemistry and Photobiology a: Chemistry. 200: 346-355. DOI: 10.1016/j.jphotochem.2008.08.006 |
0.449 |
|
2007 |
Yao Z, Bhaumik J, Dhanalekshmi S, Ptaszek M, Rodriguez PA, Lindsey JS. Synthesis of porphyrins bearing 1-4 hydroxymethyl groups and other one-carbon oxygenic substituents in distinct patterns. Tetrahedron. 63: 10657-10670. PMID 18037972 DOI: 10.1016/J.Tet.2007.07.108 |
0.571 |
|
2007 |
Muthiah C, Bhaumik J, Lindsey JS. Rational routes to formyl-substituted chlorins. The Journal of Organic Chemistry. 72: 5839-42. PMID 17585826 DOI: 10.1021/Jo0707885 |
0.552 |
|
2006 |
Bhaumik J, Yao Z, Borbas KE, Taniguchi M, Lindsey JS. Masked imidazolyl-dipyrromethanes in the synthesis of imidazole-substituted porphyrins. The Journal of Organic Chemistry. 71: 8807-17. PMID 17081010 DOI: 10.1021/Jo061461R |
0.614 |
|
2005 |
Ptaszek M, Bhaumik J, Kim HJ, Taniguchi M, Lindsey JS. Refined Synthesis of 2,3,4,5-Tetrahydro-1,3,3-trimethyldipyrrin, a Deceptively Simple Precursor to Hydroporphyrins. Organic Process Research & Development. 9: 651-659. PMID 19132135 DOI: 10.1021/Op050087E |
0.579 |
|
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