Development and Cycloaddition Reactivity of a New Class of Pyridine-Based Mesoionic 1,3-Dipole-Reference-Cited by-同舟云学术

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Development and Cycloaddition Reactivity of a New Class of Pyridine-Based Mesoionic 1,3-Dipole

Published:2016-12-22 Issue:22 Volume:129 Page:6174-6178
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Erguven Huseyin¹,Leitch David C.¹,Keyzer Evan N.¹,Arndtsen Bruce A.¹^ORCID

Affiliation:

1. Department of Chemistry; McGill University; 801 Sherbrooke St. W Montreal Quebec H3A 0B8 Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Fonds de Recherche du Québec - Nature et Technologies

Publisher

Wiley

Subject

General Medicine

Reference91 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

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1. Theoretical studies of cycloaddition reactions involving C − C triple bonds;International Reviews in Physical Chemistry;2023-10-02

2. Synthetic Strategies for the Construction of Indolizines and Indolizine‐fused Compounds: Thienoindolizines and Indolizinoindoles;Asian Journal of Organic Chemistry;2023-09-08

3. Synthesis of stable class 5 mesoionic benzo[c]tetrazolo[2,3-a]cinnolinium thiolate, dicyanomethylide, and amides;Organic & Biomolecular Chemistry;2023

4. Bicyclic 5-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: One Extra Heteroatom 1:0;Comprehensive Heterocyclic Chemistry IV;2022

5. Palladium catalyzed synthesis of indolizines via the carbonylative coupling of bromopyridines, imines and alkynes;Chemical Science;2021

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