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mom protecting group

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Chem., 2003, In contrast biomimetic synthesis does not employ protective groups. Learn about our remote access options, Department of Chemistry, University of Pittsburgh, Pittsburgh, PA 15260 USA. https://en.wikipedia.org/w/index.php?title=Protecting_group&oldid=983085830, Creative Commons Attribution-ShareAlike License. Use the link below to share a full-text version of this article with your friends and colleagues. of phenolic methoxymethyl (MOM) ethers at room temperature using , +–, , , , , , , , ,. Kollam 690525, Kerala, India, Journal Name: Letters in Organic Chemistry. Chem., 2008,

Title:A Rapid, Solvent-Free Deprotection of Methoxymethyl (MOM) Ethers by pTSA; An Eco-Friendly Approach, Affiliation:Department of Phytochemistry, Amrita School of Biotechnology, Amrita University, Clappana P.O. Recently, Lee et al. The full text of this article hosted at iucr.org is unavailable due to technical difficulties. In organic synthesis, it is used for introducing the methoxymethyl (MOM) protecting group, and is … For example, lithium aluminium hydride is a highly reactive but useful reagent capable of reducing esters to alcohols. with trifluoroacetic acid). Department of Phytochemistry, Amrita School of Biotechnology, Amrita University, Clappana P.O. Abstract:Background: Ease of preparation and alkaline stability of methoxymethyl (MOM) makes it shikimic acid for oseltamivir). Kollam 690525, Kerala, India, Current Drug Targets - Infectious Disorders, Medicinal Chemistry Reviews - Online (Discontinued), Optimizing Gene Silencing Strategies for Pancreatic Cancer, Design, Synthesis and Biological Evaluation of Carbazole Derivatives as Antitubercular and Antibacterial Agents, Unexploited Viral and Host Targets for the Treatment of Human Immunodeficiency Virus Type 1 Infection, Cancer Vaccines for Hormone/Growth Factor Immune Deprivation:A Feasible Approach for Cancer Treatment, The Anabolic Effects of Growth Hormone (GH) and GH Secretagogues on Bone Mass and Density, Computational Modeling Methods for QSAR Studies on HIV-1 Integrase Inhibitors (2005-2010), New Insights into the Chemistry and Antioxidant Activity of Coumarins, Modified Polysaccharides as Carriers for Biomolecules, An MDR-EGFP Gene Fusion Allows for Direct Cellular Localization, Function and Stability Assessment of P-Glycoprotein, Nucleoside Transport as a Potential Target for Chemotherapy in Malaria, A Facile Route for the Regioselective Deacetylation of Peracetylated Carbohydrates at Anomeric Position, Synthesis of Bisquaternary Symmetric - X,δ-Bis(2-Hydroxyiminomethylpyridinium) Alkane Dibromides and Their Reactivation of Cyclosarin-Inhibited Acetylcholinesterase, One-Pot Synthesis of 1,2,3-Triazoles from Benzyl and Alkyl Halides, Sodium Azide and Alkynes in Water Under Transition-Metal-Catalyst Free Reaction Conditions, Comparison of Novel Tacrine and 7-MEOTA Derivatives with Aromatic and Alicyclic Residues: Synthesis, Biological Evaluation and Docking Studies, Synthesis and Spectral Study of Some Novel Oxime Esters Derived from 3-azabicyclo[3.3.1]nonan-9-one Oxime, A Mild and Green Method for the N-BOC Protection of Amines without Assistant of Catalyst Under Solvent-free Conditions, Application of Amine-based Ru Compounds in the Olefin Metathesis of Methyl Eugenol: A Comparison with Grubbs Catalysts, Synthesis and Voltammetric Behavior of Loracarbef Metal Complexes, Synthesis, Crystal Structure, Luminescence, and Nonlinear Optical Properties of 2-[(E)-[[4-[2-(4-Methoxyphenyl)ethynyl]phenyl] imino]methyl]-4- [(E)-phenyldiazenyl]phenol, Synthesis of TFA-protected α-Amino Acid Chloride via a Vilsmeier Reagent for Friedel–Crafts Acylation.

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