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Yongjia Shang

Researcher at Anhui Normal University

Publications -  137
Citations -  2009

Yongjia Shang is an academic researcher from Anhui Normal University. The author has contributed to research in topics: Catalysis & Diazo. The author has an hindex of 21, co-authored 126 publications receiving 1584 citations. Previous affiliations of Yongjia Shang include Zhejiang University & Nanjing University.

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Iron metabolism regulates p53 signaling through direct heme-p53 interaction and modulation of p53 localization, stability, and function.

TL;DR: It is reported that the tumor suppressor protein p53 is downregulated during iron excess, identifying a direct link between iron/heme homeostasis and the regulation of p53 signaling, which provides mechanistic insights into iron-excess-associated tumorigenesis but may also help predict and improve outcomes in iron-deprivation-based chemotherapy.
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Syntheses, Structures, and Photoluminescence of Five New Metal−Organic Frameworks Based on Flexible Tetrapyridines and Aromatic Polycarboxylate Acids

TL;DR: In this article, tetrakis(4-pyridyloxymethylene)methane (TPOM) with deprotonated 1,4-benzenedicarboxylate (H2BDc) or 5-hydroxyisophthalic acid (5-OH-H2bdc) were characterized by elemental analysis, IR spectroscopy, and X-ray single-crystal diffraction.
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Syntheses, Structures, and Photochemical Properties of Six New Metal−Organic Frameworks Based on Aromatic Dicarboxylate Acids and V-Shaped Imidazole Ligands

TL;DR: In this paper, a 3D framework constructed from 4,4′-bis(imidazol-1-yl)diphenyl ether (BIDPE) with deprotonated 1,4-benzenedicarboxylic acid (H2bdc) in the presence of cadmium, zinc, cobalt, nickel, and manganese salts in H 2O or H2O/DMF yielded six new complexes.
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Collective total synthesis of englerin A and B, orientalol E and F, and oxyphyllol: application of the organocatalytic [4+3] cycloaddition reaction.

TL;DR: In this article, a concise collective total synthesis of englerinA and B, orientalolE and F, and oxyphyllol has been achieved in 1015 steps.
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Synthesis of Isocoumarins from Cyclic 2-Diazo-1,3-diketones and Benzoic Acids via Rh(III)-Catalyzed C-H Activation and Esterification.

TL;DR: A mild and efficient Rh(III)-catalyzed C-H activation/esterification reaction for the synthesis of isocoumarins has been developed and provides a facile approach for the construction ofIsocou marins containing various functional groups that does not require any additives.