Novel synthesis of enantiomerically pure natural inositols and their diastereomers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Micro-injection of inositol 1,3,4,5-tetrakisphosphate activates sea urchin eggs by a mechanism dependent on external Ca2+
2. Inositol Hexakisphosphate (Phytic Acid) Enhances Ca2+Influx and D-[3H]Aspartate Release in Cultured Cerebellar Neurons
3. Characterization of inositol 1,4,5-trisphosphate- and inositol 1,3,4,5-tetrakisphosphate-binding sites in rat cerebellum
4. Photoaffinity labeling and characterization of isolated inositol 1,3,4,5-tetrakisphosphate- and inositol hexakisphosphate-binding proteins.
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1. Protecting-Group-Mediated Diastereoselective Synthesis of C4′-Methylated Uridine Analogs and Their Activity against the Human Respiratory Syncytial Virus;The Journal of Organic Chemistry;2020-02-10
2. The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes;Tetrahedron;2013-06
3. Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol;Tetrahedron Letters;2011-07
4. Methyl jasmonate- and salicylic acid-induced d-chiro-inositol production in suspension cultures of buckwheat (Fagopyrum esculentum);Plant Cell, Tissue and Organ Culture (PCTOC);2011-03-23
5. ChemInform Abstract: Novel Synthesis of Enantiomerically Pure Natural Inositols and Their Diastereomers.;ChemInform;2010-06-17
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