Dioxolane acetal ring expansion during a sugar triflate displacement. Synthesis and assignment of diastereoisomer configuration of novel 9-crown-3 ether derivatives-Reference-Cited by-同舟云学术

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Dioxolane acetal ring expansion during a sugar triflate displacement. Synthesis and assignment of diastereoisomer configuration of novel 9-crown-3 ether derivatives

Published:1999-04 Issue:18 Volume:40 Page:3629-3632
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Popsavin Velimir,Berić Ostoja,Popsavin Mirjana,Csanádi János,Vujić Djura,Hrabal Richard

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. Synthesis and Reactions of Carbohydrate Trifluoro-Methanesulfonates (Carbohydrate Triplates)

2. Stereospecific Synthesis of (-)-allo-Muscarine from D-Glucose: Novel Routes to the Key Chiral Synthon

3. An alternative synthesis of (+)-epiallo-muscarine from d-glucose

4. Perfluoroalkanesulfonic Esters: Methods of Preparation and Applications in Organic Chemistry

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of higher-membered heterocycles;Synthetic Communications;2023-01-29

2. Annulative Dimerization of Carbohydrates: Synthesis of Complex C 2 ‐Symmetrical 1,4‐Dioxane‐Sugar Hybrids;European Journal of Organic Chemistry;2021-06-14

3. Neighboring-Group Participation Involving the Oxygen Atom of the O,O- or O,N-acetal Functional Groups;Current Organic Chemistry;2010-08-01

4. Rearrangements in the Course of Nucleophilic Substitution Reactions;Topics in Current Chemistry;2001

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