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Pyridinium ylids in heterocyclic synthesis

Jan Jacobs UGent, Eva Van Hende UGent, Sven Claessens UGent and Norbert De Kimpe UGent (2011) CURRENT ORGANIC CHEMISTRY. 15(9). p.1340-1362
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.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
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
journal title
CURRENT ORGANIC CHEMISTRY
Curr. Org. Chem.
volume
15
issue
9
pages
1340 - 1362
Web of Science type
Article
Web of Science id
000290610200007
JCR category
CHEMISTRY, ORGANIC
JCR impact factor
3.064 (2011)
JCR rank
15/56 (2011)
JCR quartile
2 (2011)
ISSN
1385-2728
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
1265566
handle
http://hdl.handle.net/1854/LU-1265566
date created
2011-06-16 11:12:22
date last changed
2011-06-20 16:42:27
@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},
  keyword      = {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},
}

Chicago
Jacobs, Jan, Eva Van Hende, Sven Claessens, and Norbert De Kimpe. 2011. “Pyridinium Ylids in Heterocyclic Synthesis.” Current Organic Chemistry 15 (9): 1340–1362.
APA
Jacobs, Jan, Van Hende, E., Claessens, S., & De Kimpe, N. (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.
MLA
Jacobs, Jan, Eva Van Hende, Sven Claessens, et al. “Pyridinium Ylids in Heterocyclic Synthesis.” CURRENT ORGANIC CHEMISTRY 15.9 (2011): 1340–1362. Print.