- Author
- Jan Jacobs (UGent) , Eva Van Hende (UGent) , Sven Claessens (UGent) and Norbert De Kimpe (UGent)
- Organization
- Abstract
- Pyridinium ylids are versatile tools in organic synthesis. The stability of pyridinium ylids and their generation is commented. This review gives an overview of the possible modes through which pyridinium ylids can react. It is demonstrated that pyridinium ylids are suitable building blocks for the synthesis of indolizines, cyclopropanes, 2,3-dihydrofurans, 2(1H)-pyridin(ethio)ones, mono- & oligopyridines, pyranonaphthoquinones, nitrones and azepines.
- Keywords
- indolizines, Pyridinium ylid, nitrones, pyranonaphthoquinones, pyridines, 1, 3-DIPOLAR CYCLOADDITION REACTIONS, STYRYL FLUORESCENT DYES, D-ORBITAL RESONANCE, ONE-POT SYNTHESIS, STEREOSELECTIVE-SYNTHESIS, N-YLIDES, SUBSTITUIERTER PYRIDINE, ACTIVATED CYCLOPROPANES, AZOMETHINE YLIDES, DIMETHYL ACETYLENEDICARBOXYLATE
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-1265566
- MLA
- Jacobs, Jan, Eva Van Hende, Sven Claessens, et al. “Pyridinium Ylids in Heterocyclic Synthesis.” CURRENT ORGANIC CHEMISTRY 15.9 (2011): 1340–1362. Print.
- APA
- Jacobs, Jan, Van Hende, E., Claessens, S., & De Kimpe, N. (2011). Pyridinium ylids in heterocyclic synthesis. CURRENT ORGANIC CHEMISTRY, 15(9), 1340–1362.
- Chicago author-date
- Jacobs, Jan, Eva Van Hende, Sven Claessens, and Norbert De Kimpe. 2011. “Pyridinium Ylids in Heterocyclic Synthesis.” Current Organic Chemistry 15 (9): 1340–1362.
- Chicago author-date (all authors)
- Jacobs, Jan, Eva Van Hende, Sven Claessens, and Norbert De Kimpe. 2011. “Pyridinium Ylids in Heterocyclic Synthesis.” Current Organic Chemistry 15 (9): 1340–1362.
- Vancouver
- 1.Jacobs J, Van Hende E, Claessens S, De Kimpe N. Pyridinium ylids in heterocyclic synthesis. CURRENT ORGANIC CHEMISTRY. 2011;15(9):1340–62.
- IEEE
- [1]J. Jacobs, E. Van Hende, S. Claessens, and N. De Kimpe, “Pyridinium ylids in heterocyclic synthesis,” CURRENT ORGANIC CHEMISTRY, vol. 15, no. 9, pp. 1340–1362, 2011.
@article{1265566,
abstract = {Pyridinium ylids are versatile tools in organic synthesis. The stability of pyridinium ylids and their generation is commented. This review gives an overview of the possible modes through which pyridinium ylids can react. It is demonstrated that pyridinium ylids are suitable building blocks for the synthesis of indolizines, cyclopropanes, 2,3-dihydrofurans, 2(1H)-pyridin(ethio)ones, mono- & oligopyridines, pyranonaphthoquinones, nitrones and azepines.},
author = {Jacobs, Jan and Van Hende, Eva and Claessens, Sven and De Kimpe, Norbert},
issn = {1385-2728},
journal = {CURRENT ORGANIC CHEMISTRY},
keywords = {indolizines,Pyridinium ylid,nitrones,pyranonaphthoquinones,pyridines,1,3-DIPOLAR CYCLOADDITION REACTIONS,STYRYL FLUORESCENT DYES,D-ORBITAL RESONANCE,ONE-POT SYNTHESIS,STEREOSELECTIVE-SYNTHESIS,N-YLIDES,SUBSTITUIERTER PYRIDINE,ACTIVATED CYCLOPROPANES,AZOMETHINE YLIDES,DIMETHYL ACETYLENEDICARBOXYLATE},
language = {eng},
number = {9},
pages = {1340--1362},
title = {Pyridinium ylids in heterocyclic synthesis},
volume = {15},
year = {2011},
}