The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides-Reference-Cited by-同舟云学术

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The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides

Published:2017-12-18 Issue:3 Volume:2018 Page:262-294
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Bakulev Vasiliy A.¹,Beryozkina Tetyana¹,Thomas Joice²,Dehaen Wim³^ORCID

Affiliation:

1. Ural Federal University; Mira st. 19 620002 Yekaterinburg Russia

2. Department of Chemistry; The Bridge@USC and Loker Hydrocarbon Research Institute; University of Southern California; 90089-1661 Los Angeles CA USA

3. Molecular Design and Synthesis; Department of Chemistry; KU Leuven; Celestijnenlaan 200F 3001 Leuven Belgium

Funder

Russian Science Foundation

KU Leuven

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference212 articles.

1. Münchnones-New Facets after 50 Years

2. Münchnone - 50 Jahre und ein bisschen weiser

3. Recent advances in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides

4. Progress in 1,3-dipolar cycloadditions in the recent decade: an update to strategic development towards the arsenal of organic synthesis

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3. Synthesis and applications of fluorinated, polyfluoroalkyl- and polyfluoroaryl-substituted 1,2,3-triazoles;Organic Chemistry Frontiers;2024

4. Convergent synthesis of thiodiazole dioxides from simple ketones and amines through an unusual nitrogen-migration mechanism;Chemical Science;2024

5. Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review);Russian Journal of General Chemistry;2024-01

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