The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives

Buckley BR, Page PCB, Chan Y, Heaney H, Klaes M, McIldowie MJ, McKee V, Mattay J, Mocerino M, Moreno E, Skelton BW, et al. (2006)
European Journal of Organic Chemistry 2006(22): 5135-5151.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Buckley, Benjamin R.; Page, Philip C. Bulman; Chan, Yohan; Heaney, Harry; Klaes, Michael; McIldowie, Matthew J.; McKee, Vickie; Mattay, JochenUniBi; Mocerino, Mauro; Moreno, Eduardo; Skelton, Brian W.; White, Allan H.
Alle
Abstract / Bemerkung
The preparation of a series of diastereoisomeric tetracamphorsulfonates derived from racemic tetramethoxyresorcin[4]arenes was achieved by reactions with an excess of (S)(+)-10-camphorsulfonyl chloride in pyridine followed by isolation using flash chromatography. Tetradeprotonation of a number of tetramethoxyresorcin[4]arenes using n-butyllithium in tetrahydrofuran, followed by reactions using (S)-(+)10-camphorsulfonyl chloride, gave the same tetracamphorsulfonates. Mono-, di- and tricamphorsulfonates were also prepared following selective deprotonation. In the reactions with tetraisopropyloxy- and tetracyclopentyloxyresorcin[4]arenes, only the mono- and dicamphorsulfonates were formed. X-ray crystallographic analysis established the absolute configurations of three diastereoisomerically pure tetracamphorsulfonates, including a diastereoisomer prepared from 6,12,18,24-tetramethoxy-2,8,14,20-tetrakis(2-methylpropyl)resorcin[4]are ne. An additional pair of diastereoisomers was also prepared using (R)-(-)-10-camphorsulfonyl chloride and 6,12,18,24-tetramethoxy-2,8,14,20-tetrakis(2-methylpropyl)resorcin[4]are ne, for one of which the structure was confirmed by an additional X-ray structure determination. Hydrolytic removal of the camphorsulfonyl residue(s) from the various diastereoisomers gave enantiomers of known absolute configurations. In some cases, the chiral nonracemic tetraalkoxyresorcin[4]arenes were converted into known tetrabenzoxazine derivatives by using N,N-bis(methoxymethyl)[(S)-(-)-(a-methylbenzyl)]amine in thermal or microwave - assisted reactions. (c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006.
Stichworte
camphorsulfonates; chiral auxiliaries; configuration; diastereoselectivity; determination; hydrolysis; resorcin[4]arenes; axial chirality; Mannich reactions
Erscheinungsjahr
2006
Zeitschriftentitel
European Journal of Organic Chemistry
Band
2006
Ausgabe
22
Seite(n)
5135-5151
ISSN
1434-193X
eISSN
1099-0690
Page URI
https://pub.uni-bielefeld.de/record/1596920

Zitieren

Buckley BR, Page PCB, Chan Y, et al. The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives. European Journal of Organic Chemistry. 2006;2006(22):5135-5151.
Buckley, B. R., Page, P. C. B., Chan, Y., Heaney, H., Klaes, M., McIldowie, M. J., McKee, V., et al. (2006). The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives. European Journal of Organic Chemistry, 2006(22), 5135-5151. https://doi.org/10.1002/ejoc.200600591
Buckley, Benjamin R., Page, Philip C. Bulman, Chan, Yohan, Heaney, Harry, Klaes, Michael, McIldowie, Matthew J., McKee, Vickie, et al. 2006. “The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives”. European Journal of Organic Chemistry 2006 (22): 5135-5151.
Buckley, B. R., Page, P. C. B., Chan, Y., Heaney, H., Klaes, M., McIldowie, M. J., McKee, V., Mattay, J., Mocerino, M., Moreno, E., et al. (2006). The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives. European Journal of Organic Chemistry 2006, 5135-5151.
Buckley, B.R., et al., 2006. The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives. European Journal of Organic Chemistry, 2006(22), p 5135-5151.
B.R. Buckley, et al., “The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives”, European Journal of Organic Chemistry, vol. 2006, 2006, pp. 5135-5151.
Buckley, B.R., Page, P.C.B., Chan, Y., Heaney, H., Klaes, M., McIldowie, M.J., McKee, V., Mattay, J., Mocerino, M., Moreno, E., Skelton, B.W., White, A.H.: The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives. European Journal of Organic Chemistry. 2006, 5135-5151 (2006).
Buckley, Benjamin R., Page, Philip C. Bulman, Chan, Yohan, Heaney, Harry, Klaes, Michael, McIldowie, Matthew J., McKee, Vickie, Mattay, Jochen, Mocerino, Mauro, Moreno, Eduardo, Skelton, Brian W., and White, Allan H. “The preparation and absolute configurations of enantiomerically pure C-4-symmetric tetraalkoxyresorcin[4]arenes obtained from camphorsulfonate derivatives”. European Journal of Organic Chemistry 2006.22 (2006): 5135-5151.
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