アルソール (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "アルソール" in Japanese language version.

refsWebsite

Global rank Japanese rank

7doi.org

2^nd place

6^th place

5books.google.com

3^rd place

61^st place

2bris.ac.uk

4,848^th place

low place

1nih.gov

4^th place

24^th place

1qmul.ac.uk

1,735^th place

2,576^th place

books.google.com

Frederick George Mann (1970). The heterocyclic derivatives of phosphorus, arsenic, antimony, and bismuth. John Wiley and Sons. pp. 357-360. ISBN 978-0-471-37489-3 2011年3月21日閲覧. "In English this ring system has frequently named arsenole 'for euphony'"
Nicholas C. Norman (1998). Chemistry of arsenic, antimony, and bismuth. Springer. p. 235. ISBN 978-0-7514-0389-3 2011年3月15日閲覧。
Richard Watson Todd (25 May 2007). Much ado about English: up and down the bizarre byways of a fascinating language. Nicholas Brealey Publishing. p. 138. ISBN 978-1-85788-372-5 2011年3月15日閲覧。
Tadeusz Marek Krygowski; Michal K. Cyra?ski; M. Agostinha R. Matos (2009). Aromaticity in Heterocyclic Compounds. Springer. pp. 47-. ISBN 978-3-540-68329-2 2011年3月21日閲覧。
C. W. Bird; Gordon William Henry Cheeseman (31 December 1973). Aromatic and Heteroatomic Chemistry. Royal Society of Chemistry. pp. 23-. ISBN 978-0-85186-753-3 2011年3月23日閲覧。

bris.ac.uk

chm.bris.ac.uk

Paul W May, Molecules with Silly or Unusual Names, publ. 2008 Imperial College Press, ISBN 978-1-84816-207-5(pbk). See also the Web page "Molecules with Silly or Unusual Names" at the School of Chemistry, University of Bristol, (retrieved 29 Sept 2008)
Gottfried Markl & Hagen Hauptmann (1972). “Unusual Substitution in an Arsole Ring”. Angewandte Chemie International Edition in English 11: 441. doi:10.1002/anie.197204411.

doi.org

M. P. Johansson; J. Juselius (2005). “Arsole Aromaticity Revisited”. Lett. Org. Chem. 2: 469-474. doi:10.2174/1570178054405968. "Using quantum chemical methodology, we reinvestigate the aromaticity of the much debated arsole, using the newly developed gauge-including magnetically induced currents (GIMIC) method. GIMIC provides a quantitative measure of the induced ring current strength, showing arsole to be moderately aromatic."
A. Muranaka; S. Yasuike; C-Y. Liu; J. Kurita; N. Kakusawa; T. Tsuchiya; M. Okuda; N. Kobayashi et al. (2009). “Effect of Periodic Replacement of the Heteroatom on the Spectroscopic Properties of Indole and Benzofuran Derivatives”. J. Phys. Chem. A 113 (2): 464-473. doi:10.1021/jp8079843. PMID 19099440.
Pelzer, Silke; Wichmann, Karin; Wesendrup, Ralf; Schwerdtfeger, Peter (2002). “Trends in Inversion Barriers IV. The Group 15 Analogous of Pyrrole”. The Journal of Physical Chemistry A 106: 6387. doi:10.1021/jp0203494.
Pelloni, Stefano; Lazzeretti, Paolo (2007). “Magnetotropicity of phosphole and its arsenic analogue”. Theoretical Chemistry Accounts 118: 89. doi:10.1007/s00214-007-0247-0.
Braye, E. H.; Hubel, W.; Caplier, I. (1961). “New Unsaturated Heterocyclic Systems. I”. Journal of the American Chemical Society 83: 4406. doi:10.1021/ja01482a026.
Gottfried Markl & Hagen Hauptmann (1972). “Unusual Substitution in an Arsole Ring”. Angewandte Chemie International Edition in English 11: 441. doi:10.1002/anie.197204411.
Markl, G (1983). “Synthese von 1-phenyl-2,5-diaryl(dialkyl)-arsolen; umsetzung der arsole mit alkalimetallen und lithiumorganylen”. Journal of Organometallic Chemistry 249: 335. doi:10.1016/S0022-328X(00)99433-6.

nih.gov

pubmed.ncbi.nlm.nih.gov

A. Muranaka; S. Yasuike; C-Y. Liu; J. Kurita; N. Kakusawa; T. Tsuchiya; M. Okuda; N. Kobayashi et al. (2009). “Effect of Periodic Replacement of the Heteroatom on the Spectroscopic Properties of Indole and Benzofuran Derivatives”. J. Phys. Chem. A 113 (2): 464-473. doi:10.1021/jp8079843. PMID 19099440.

qmul.ac.uk

chem.qmul.ac.uk

"Revision of the Extended Hantzsch-Widman System of Nomenclature for Heteromonocycles" at IUPAC, retrieved 29 Sept 2008