Two diamino-substituted lithiocarbanions in one molecule

Kamps I, Mix A, Berger R, Neumann B, Stammler H-G, Mitzel NW (2009)
CHEMICAL COMMUNICATIONS (37): 5558-5560.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
DOI
Autor*in
Kamps, Ina; Mix, AndreasUniBi; Berger, RaphaelUniBi ; Neumann, BeateUniBi; Stammler, Hans-GeorgUniBi; Mitzel, Norbert W.UniBi
Einrichtung
Fakultät für Chemie > Anorganische Chemie und Strukturchemie
Abstract / Bemerkung
tert-Butyllithium deprotonates bis(3-methyl-1,3-diazacyclohex-1-yl)-methane and its five-ring analogue regioselectively at both endocyclic NCH2N units; a deprotonation intermediate has been isolated and structurally characterised.
Erscheinungsjahr
2009
Zeitschriftentitel
CHEMICAL COMMUNICATIONS
Ausgabe
37
Seite(n)
5558-5560
ISSN
1359-7345
eISSN
1364-548X
Page URI
https://pub.uni-bielefeld.de/record/1590912

Zitieren

Kamps I, Mix A, Berger R, Neumann B, Stammler H-G, Mitzel NW. Two diamino-substituted lithiocarbanions in one molecule. CHEMICAL COMMUNICATIONS. 2009;(37):5558-5560.
Kamps, I., Mix, A., Berger, R., Neumann, B., Stammler, H. - G., & Mitzel, N. W. (2009). Two diamino-substituted lithiocarbanions in one molecule. CHEMICAL COMMUNICATIONS(37), 5558-5560. https://doi.org/10.1039/b909561f
Kamps, Ina, Mix, Andreas, Berger, Raphael, Neumann, Beate, Stammler, Hans-Georg, and Mitzel, Norbert W. 2009. “Two diamino-substituted lithiocarbanions in one molecule”. CHEMICAL COMMUNICATIONS, no. 37: 5558-5560.
Kamps, I., Mix, A., Berger, R., Neumann, B., Stammler, H. - G., and Mitzel, N. W. (2009). Two diamino-substituted lithiocarbanions in one molecule. CHEMICAL COMMUNICATIONS, 5558-5560.
Kamps, I., et al., 2009. Two diamino-substituted lithiocarbanions in one molecule. CHEMICAL COMMUNICATIONS, (37), p 5558-5560.
I. Kamps, et al., “Two diamino-substituted lithiocarbanions in one molecule”, CHEMICAL COMMUNICATIONS, 2009, pp. 5558-5560.
Kamps, I., Mix, A., Berger, R., Neumann, B., Stammler, H.-G., Mitzel, N.W.: Two diamino-substituted lithiocarbanions in one molecule. CHEMICAL COMMUNICATIONS. 5558-5560 (2009).
Kamps, Ina, Mix, Andreas, Berger, Raphael, Neumann, Beate, Stammler, Hans-Georg, and Mitzel, Norbert W. “Two diamino-substituted lithiocarbanions in one molecule”. CHEMICAL COMMUNICATIONS 37 (2009): 5558-5560.

2 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Three different product types from reactions of lithiated cyclic aminals with trivalent organometal chlorides.
Hellmann BJ, Kamps I, Mix A, Neumann B, Stammler HG, Mitzel NW., Chem. Commun. (Camb.) 46(35), 2010
PMID: 20714557
Unexpected direct dilithiation of a prochiral phosphine borane.
Gessner VH, Dilsky S, Strohmann C., Chem. Commun. (Camb.) 46(26), 2010
PMID: 20485825

28 References

Daten bereitgestellt von Europe PubMed Central.


Bordwell, J. Am. Chem. Soc. 113(), 1991

Gessner, Chem.–Eur. J. 15(), 2009

Seyferth, J. Org. Chem. 24(), 1959

Peterson, Organomet. Chem. Rev., Sect. A 7(), 1972

Peterson, J. Am. Chem. Soc. 93(), 1971

Peterson, J. Organomet. Chem. 21(), 1970

Tian, Organometallics 24(), 2005

Tian, Organometallics 24(), 2005

Gawley, J. Org. Chem. 60(), 1995

Quintard, Synthesis (), 1984

Strohmann, Angew. Chem. 108(), 1996
Lewis Acid Complexation of Tertiary Amines and Related Compounds: A Strategy for alpha-Deprotonation and Stereocontrol.
Kessar SV, Singh P., Chem. Rev. 97(3), 1997
PMID: 11848886

Arnold, J. Chem. Soc., Dalton Trans. (), 2002

Schlosser, Angew. Chem. 85(), 1973

Bauer, J. Am. Chem. Soc. 114(), 1992

Köhler, Chem. Ber. 120(), 1987
Lithiation of TMEDA and its higher homologous TEEDA: understanding observed alpha- and beta-deprotonation.
Gessner VH, Strohmann C., J. Am. Chem. Soc. 130(44), 2008
PMID: 18842047

Gessner, Angew. Chem. 119(), 2007

Strohmann, Angew. Chem. 119(), 2007

Bojer, Angew. Chem. 119(), 2007

Köhn, Chem. Ber. 129(), 1996

Seebach, J. Org. Chem. 40(), 1975

Karsch, Chem. Ber. 129(), 1996
A precoordination complex of 1,2,3-trimethyl-1,3,5-triazacyclohexane with tert-butyllithium as key intermediate in its methylene group deprotonation.
Strohmann C, Gessner VH., Chem Asian J 3(11), 2008
PMID: 18752226

Whisler, Angew. Chem. 116(), 2004

Keresztes, J. Am. Chem. Soc. 122(), 2000
Simple and efficient fabrication of room temperature stable electride: melt-solidification and glass ceramics.
Kim S, Miyakawa M, Hayashi K, Sakai T, Hirano M, Hosono H., J. Am. Chem. Soc. 127(5), 2005
PMID: 15686358

Spek, Acta Crystallogr., Sect. A 46(), 1990
Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®
Quellen

PMID: 19753356
PubMed | Europe PMC

Suchen in

Google Scholar