An efficient and highly diastereoselective synthesis of C-glycosylated 1,3-oxazolidines from N-methyl-d-glucamine-Reference-Cited by-同舟云学术

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An efficient and highly diastereoselective synthesis of C-glycosylated 1,3-oxazolidines from N-methyl-d-glucamine

Published:2008-06 Issue:27 Volume:64 Page:6377-6386
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Martínez R. Fernando,Ávalos Martín,Babiano Reyes,Cintas Pedro,Jiménez José L.,Light Mark E.,Palacios Juan C.,Pérez Esther M.S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference38 articles.

1. Replacing the Nucleobases in DNA with Designer Molecules

2. 2‐ C ‐Formyl Glycals: Emerging Chiral Synthons in Organic Synthesis

3. Beyond A, C, G and T: augmenting nature's alphabet

4. First Synthesis of Double Headed 1,3,4‐Oxadiazino[6,5‐b]indole AcycloC‐Nucleosides

5. A Review: Synthesis of ArylC-Glycosides Via the Heck Coupling Reaction

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1. Exploring and Re-Assessing Reverse Anomeric Effect in 2-Iminoaldoses Derived from Mono- and Polynuclear Aromatic Aldehydes;Molecules;2024-08-30

2. A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect in 2-Iminoaldoses;The Journal of Organic Chemistry;2024-05-16

3. Schiff Bases and Stereocontrolled Formation of Fused 1,3-Oxazolidines from 1-Amino-2-Indanol: A Systematic Study on Structure and Mechanism;Molecules;2023-02-09

4. Amphipathic 1,3-oxazolidines from N-alkyl glucamines and benzaldehydes: stereochemical and mechanistic studies;New Journal of Chemistry;2021

5. Electronic effects in tautomeric equilibria: the case of chiral imines from d-glucamine and 2-hydroxyacetophenones;Organic & Biomolecular Chemistry;2019

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