A highly diastereoselective [3+3] annulation reaction of aza-oxyallyl cations and nitrones-Reference-Cited by-同舟云学术

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A highly diastereoselective [3+3] annulation reaction of aza-oxyallyl cations and nitrones

Published:2018-05 Issue:20 Volume:59 Page:1916-1920
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Chen Rongxing,Sun Shaofa,Wang Gangqiang,Guo Haibing

Funder

Hubei Provincial Department of Education

Hubei Provincial Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference43 articles.

1. A New Synthesis of N-Alkoxy-2-ethoxyarylacetamides from N-Alkoxy-N-chloroarylacetamides with Triethylamine in Ethanol.

2. Angew Chem;Lengyel;Int Ed,1968

3. Trapping the elusive aza-oxyallylic cation: new opportunities in heterocycloaddition chemistry

4. Generation and Reactivity of Aza-Oxyallyl Cationic Intermediates: Aza-[4 + 3] Cycloaddition Reactions for Heterocycle Synthesis

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1. α‐Halocarbonyls as a Valuable Functionalized Tertiary Alkyl Source;ChemistryOpen;2024-07-11

2. Aza‐oxyallyl Cations and Their Applications in (3+m) Cycloaddition Reactions;European Journal of Organic Chemistry;2022-11-09

3. 1,2,4-Oxadiazines and 1,2,4-Thiadiazines;Comprehensive Heterocyclic Chemistry IV;2022

4. One‐Pot Synthesis of Fused Indolin‐3‐Ones via a [3+3] Cycloaddition Reaction;Advanced Synthesis & Catalysis;2021-09-23

5. 1,3-Dipolar cycloaddition of nitrones: synthesis of multisubstituted, diverse range of heterocyclic compounds;New Journal of Chemistry;2021

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