Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference72 articles.
1. Discovery of a Catalytic Asymmetric Phosphorylation through Selection of a Minimal Kinase Mimic: A Concise Total Synthesis of d-myo-Inositol-1-Phosphate
2. Enantiodivergence in Small-Molecule Catalysis of Asymmetric Phosphorylation: Concise Total Syntheses of the Enantiomeric d-myo-Inositol-1-phosphate and d-myo-Inositol-3-phosphate
3. Regioselective Protection and Deprotection of Inositol Hydroxyl Groups
4. Establishment of the Structure of Pinpollitol by Total Synthesis of the Proposed Putative Structures
5. Regioselective one-pot protection of carbohydrates
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1. Inositol Adenophostin: Convergent Synthesis of a Potent Agonist of d-myo-Inositol 1,4,5-Trisphosphate Receptors;ACS Omega;2020-10-28
2. Recent developments in the synthesis of biologically relevant inositol derivatives;Carbohydrates in Drug Discovery and Development;2020
3. Rigid triol and diol with adamantane-like core derived from naturally occurringmyo-inositol and their polyaddition with diisocyanates;Journal of Polymer Science Part A: Polymer Chemistry;2014-10
4. Triallyl monomer bearing adamantane-like core derived from naturally occurring myo -inositol: Synthesis and polyaddition with dithiols;Journal of Polymer Science Part A: Polymer Chemistry;2014-02-04
5. The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes;Tetrahedron;2013-06
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