Year |
Citation |
Score |
2023 |
Das P, Thakur R. Amino-Acid-Derived Amides as Stereodirecting Leaving Groups for Ferrier Rearrangement via Pd(0)-Catalyzed Tsuji-Trost Reactions. Organic Letters. 25: 6046-6051. PMID 37556780 DOI: 10.1021/acs.orglett.3c02226 |
0.699 |
|
2021 |
Thakur R, Das P, Molla MR, Kumar A. o-Cyanobenzoate: A Recyclable and Reusable Stereodirecting Group for β-O-Glycosylation via Pd(0)-Catalyzed Ferrier Rearrangement. Chemistry, An Asian Journal. PMID 34866348 DOI: 10.1002/asia.202101156 |
0.734 |
|
2021 |
Gholap SS, Dakhil AA, Chakraborty P, Li H, Dutta I, Das PK, Huang KW. Efficient and chemoselective hydrogenation of aldehydes catalyzed by well-defined PN-pincer manganese(II) catalyst precursors: an application in furfural conversion. Chemical Communications (Cambridge, England). PMID 34693946 DOI: 10.1039/d1cc04808b |
0.309 |
|
2021 |
Mao Q, Das PK, Le Gac S, Boitrel B, Dorcet V, Oohora K, Hayashi T, Kitagishi H. Functional Myoglobin Model Composed of a Strapped Porphyrin/Cyclodextrin Supramolecular Complex with an Overhanging COOH That Increases O/CO Binding Selectivity in Aqueous Solution. Inorganic Chemistry. PMID 34319113 DOI: 10.1021/acs.inorgchem.1c01628 |
0.337 |
|
2020 |
Molla MR, Das P, Guleria K, Subramanian R, Kumar A, Thakur R. Cyanomethyl ether as an Orthogonal Participating Group for Stereoselective Synthesis of 1,2-Trans-β-O-Glycosides. The Journal of Organic Chemistry. PMID 32600042 DOI: 10.1021/Acs.Joc.0C01249 |
0.427 |
|
2017 |
Chakraborty C, Samadder S, Roychowdhury A, Roy A, Das P, Mandal RK, Roychoudhury S, Panda CK. Activation of Wnt-β-catenin pathway in basal-parabasal layers of normal cervical epithelium comparable during development of uterine cervical carcinoma. Molecular and Cellular Biochemistry. PMID 29079964 DOI: 10.1007/s11010-017-3216-5 |
0.312 |
|
2015 |
Amanullah S, Das PK, Samanta S, Dey A. Tuning the thermodynamic onset potential of electrocatalytic O2 reduction reaction by synthetic iron-porphyrin complexes. Chemical Communications (Cambridge, England). 51: 10010-3. PMID 26000662 DOI: 10.1039/C5Cc01938A |
0.3 |
|
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