2,6,9-Triazabicyclo[3.3.1]nonanes as overlooked amino-modification products by acrolein
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2013/OB/C3OB41285G
Reference22 articles.
1. New strategy in synthetic biology: from enzyme inhibition and natural products synthesis to PET imaging by 6π-azaelectrocyclization
2. Exploring a Unique Reactivity of 6π-Azaelectrocyclization to Enzyme Inhibition, Natural Products Synthesis, and Molecular Imaging: An Approach to Chemical Biology by Synthetic Chemists
3. Conjugated imines and iminium salts as versatile acceptors of nucleophiles
4. A Submicrogram-Scale Protocol for Biomolecule-Based PET Imaging by Rapid 6π-Azaelectrocyclization: Visualization of Sialic Acid Dependent Circulatory Residence of Glycoproteins
5. Electrocyclization-Based Labeling Allows Efficient In Vivo Imaging of Cellular Trafficking
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1. Application of Acrolein Imines to Organic Synthesis, Biofunctional Studies, and Clinical Practice;The Chemical Record;2021-03-26
2. Enantioselective synthesis of cyclic and linear diamines by imine cycloadditions;Chirality;2020-07-03
3. Selectfluor-Mediated Stereoselective [1 + 1 + 4 + 4] Dimerization of Styrylnaphthols;Organic Letters;2019-12-10
4. Chemical Sensing of Acrolein-Amine Conjugates for Food Quality Control: A Case Study of Milk Products;Bulletin of the Chemical Society of Japan;2019-06-15
5. Facile Assembling of Novel 2,3,6,7,9-pentaazabicyclo- [3.3.1]nona-3,7-diene Derivatives under Microwave and Ultrasound Platforms;Molecules;2019-03-20
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