Allylic Azide Rearrangements Investigated by Density Functional Theory Calculations-Reference-Cited by-同舟云学术

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Allylic Azide Rearrangements Investigated by Density Functional Theory Calculations

Published:2017-12 Issue:12 Volume:38 Page:1419-1426
ISSN:1229-5949
Container-title:Bulletin of the Korean Chemical Society
language:en
Short-container-title:Bull. Korean Chem. Soc.

Author:

Kang Han-Young¹,Kang Young Kee¹

Affiliation:

1. Department of Chemistry; Chungbuk National University; Cheongju Chungbuk, 28644 Korea

Funder

National Research Foundation of Korea (NRF)

Chungbuk National University

Publisher

Wiley

Subject

General Chemistry

Reference39 articles.

1. Organic Azides: An Exploding Diversity of a Unique Class of Compounds

2. REARRANGEMENT OF ALLYLIC AZIDES

3. Intramolecular OH insertion reaction of azido substituted diazoesters and its relevance to the mechanism of the allylic azide rearrangement

4. Stereocontrol in a Combined Allylic Azide Rearrangement and Intramolecular Schmidt Reaction

5. A Concomitant Allylic Azide Rearrangement/Intramolecular Azide–Alkyne Cycloaddition Sequence

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1. Progress toward the Total Synthesis of Jogyamycin Using a Tandem Ichikawa/Winstein Rearrangement;Organic Letters;2023-11-09

2. Understanding the Fate of the Banert Cascade of Propargylic Azides: Sigmatropic versus Prototropic Pathway;The Journal of Organic Chemistry;2023-07-07

3. Insight into the intramolecular interactions of trans-2-azidocycloalk-3-en-1-ols and trans-2-azidocycloalk-3-en-1-yl acetates: A theoretical study;Tetrahedron;2021-07

4. Insight into the factors controlling the equilibrium of allylic azides;RSC Advances;2020

5. Palladium‐Catalyzed Selective Three‐Component Tandem Reaction to Bicyclic 1,2,3‐Triazole Derivatives;Advanced Synthesis & Catalysis;2019-12-11

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