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Insights into the role of sialylation in cancer progression and metastasis
Upregulation of sialyltransferases—the enzymes responsible for the addition of sialic acid to
growing glycoconjugate chains—and the resultant hypersialylation of up to 40–60% of …
growing glycoconjugate chains—and the resultant hypersialylation of up to 40–60% of …
Mitsunobu and related reactions: advances and applications
The substitution of primary or secondary alcohols with nucleophiles mediated by a redox
combination of a trialkylor triarylphosphine and a dialkyl azodicarboxylate is popularly …
combination of a trialkylor triarylphosphine and a dialkyl azodicarboxylate is popularly …
[HTML][HTML] Recent advances in the development of sialyltransferase inhibitors to control cancer metastasis: A comprehensive review
Metastasis accounts for the majority of cancer-associated mortalities, representing a huge
health and economic burden. One of the mechanisms that enables metastasis is …
health and economic burden. One of the mechanisms that enables metastasis is …
The chemistry and biology of mucin-type O-linked glycosylation
Mucin-type O-linked glycosylation is a fundamental post-translational modification that is
involved in a variety of important biological processes. However, the lack of chemical tools to …
involved in a variety of important biological processes. However, the lack of chemical tools to …
An overview of stereoselective synthesis of α-aminophosphonic acids and derivatives
M Ordóñez, H Rojas-Cabrera, C Cativiela - Tetrahedron, 2009 - Elsevier
1. Introduction a-Aminoalkylphosphonic acids 1 are structurally analogous to a-amino acids
2, obtained by isosteric substitution of the planar and less bulky carboxylic acid (CO2H) by a …
2, obtained by isosteric substitution of the planar and less bulky carboxylic acid (CO2H) by a …
Asymmetric synthesis of hydroxyphosphonates
OI Kolodiazhnyi - Tetrahedron: Asymmetry, 2005 - Elsevier
Hydroxyphosphonates have attracted considerable attention as biologically active
compounds, enzyme inhibitors, and drugs. Over the last few years significant interest in the …
compounds, enzyme inhibitors, and drugs. Over the last few years significant interest in the …
Zirconium (IV) compounds as efficient catalysts for synthesis of α-aminophosphonates
S Bhagat, AK Chakraborti - The Journal of organic chemistry, 2008 - ACS Publications
Zirconium (IV) compounds are reported as excellent catalysts for a three-component one-pot
reaction of an amine, an aldehyde or a ketone, and a di/trialkyl/aryl phosphite to form α …
reaction of an amine, an aldehyde or a ketone, and a di/trialkyl/aryl phosphite to form α …
Advancement of sialyltransferase inhibitors: therapeutic challenges and opportunities
R Szabo, D Skropeta - Medicinal Research Reviews, 2017 - Wiley Online Library
Hypersialylation of tumor cell surface proteins along with a marked upregulation of
sialyltransferase (ST) activity is a well‐established hallmark of cancer. Due to the critical role …
sialyltransferase (ST) activity is a well‐established hallmark of cancer. Due to the critical role …
Glycan antagonists and inhibitors: a fount for drug discovery
JR Brown, BE Crawford, JD Esko - Critical reviews in biochemistry …, 2007 - Taylor & Francis
Glycans, the carbohydrate chains of glycoproteins, proteoglycans, and glycolipids, represent
a relatively unexploited area for drug development compared with other macromolecules …
a relatively unexploited area for drug development compared with other macromolecules …
Chiral hydroxy phosphonates: synthesis, configuration and biological properties
OI Kolodiazhnyi - Russian Chemical Reviews, 2006 - iopscience.iop.org
Published data on the synthesis, absolute configurations and biological properties of chiral
hydroxy phosphonates are generalised and described systematically. Examples of …
hydroxy phosphonates are generalised and described systematically. Examples of …