-
3
-
-
0011106853
-
-
3. There had been considerable confusion in the literature regarding the diagrammatic representation of the absolute configuration of sphingosines. Gigg, R. H. Chem. Phys. Lipids 1969, 3, 106.
-
(1969)
Chem. Phys. Lipids
, vol.3
, pp. 106
-
-
Gigg, R.H.1
-
4
-
-
0000415968
-
-
4. The absolute configurations of sphingosines and dihydrosphingosines were established by the synthetic works: (a) Carter, H. E.; Glick, F. J.; Norris, W. P.; Philips, G. E. J. Biol. Chem. 1947, 170, 285;
-
(1947)
J. Biol. Chem.
, vol.170
, pp. 285
-
-
Carter, H.E.1
Glick, F.J.2
Norris, W.P.3
Philips, G.E.4
-
6
-
-
0011139168
-
-
(c) Carter, H. E.; Harrison, J. B.; Shapiro, D. J. Am. Chem. Soc. 1953, 75, 4705;
-
(1953)
J. Am. Chem. Soc.
, vol.75
, pp. 4705
-
-
Carter, H.E.1
Harrison, J.B.2
Shapiro, D.3
-
7
-
-
0001573799
-
-
(d) Kiss, J.; Fodor, G.; Banfi, D. Helv. Chim. Acta 1954, 37, 1471;
-
(1954)
Helv. Chim. Acta
, vol.37
, pp. 1471
-
-
Kiss, J.1
Fodor, G.2
Banfi, D.3
-
11
-
-
0011137613
-
-
5. Igarashi, Y.; Hakomori, S.; Toyokuni, T.; Dean, B.; Fujita, S.; Sugimoto, M.; Ogawa, T.; El-Ghendy, K.; Racker, E. Biochemistry 1988, 171, 373.
-
(1988)
Biochemistry
, vol.171
, pp. 373
-
-
Igarashi, Y.1
Hakomori, S.2
Toyokuni, T.3
Dean, B.4
Fujita, S.5
Sugimoto, M.6
Ogawa, T.7
El-Ghendy, K.8
Racker, E.9
-
12
-
-
0025866050
-
-
6. Mullmann, T. J.; Siegel, M. I.; Egan, R. W.; Billah, M. M. J. Biol. Chem. 1991, 200, 2013.
-
(1991)
J. Biol. Chem.
, vol.200
, pp. 2013
-
-
Mullmann, T.J.1
Siegel, M.I.2
Egan, R.W.3
Billah, M.M.4
-
14
-
-
0026651770
-
-
8. (a) Pushkareva, M. Y.; Khan, W. A.; Alessenko, A. V.; Sahyoun, N.; Hannun, Y. A. J. Biol. Chem. 1992, 267, 15246;
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 15246
-
-
Pushkareva, M.Y.1
Khan, W.A.2
Alessenko, A.V.3
Sahyoun, N.4
Hannun, Y.A.5
-
15
-
-
0027076191
-
-
(b) Chao, R.; Khan, W.; Hannun, Y. A. J. Biol. Chem. 1992, 267, 23459.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 23459
-
-
Chao, R.1
Khan, W.2
Hannun, Y.A.3
-
16
-
-
0028234366
-
-
9. Olivera, A.; Zhang, H.; Carlson, R. O.; Mattie, M. E.; Schmidt, R. R.; Spiegel, S. J. Biol. Chem. 1994, 269, 17924.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 17924
-
-
Olivera, A.1
Zhang, H.2
Carlson, R.O.3
Mattie, M.E.4
Schmidt, R.R.5
Spiegel, S.6
-
17
-
-
85047668742
-
-
10. (a) Dirsch, V.; Frederico, J.; Zhao, N.; Cai, G.; Chen, Y.; Vunnam, S.; Odingo, J.; Pu, H.; Nakanishi, K.; Berova, N.; Liotta, D.; Bielawska, A.; Hannun, Y. Tetrahedron Lett. 1995, 36, 4959;
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 4959
-
-
Dirsch, V.1
Frederico, J.2
Zhao, N.3
Cai, G.4
Chen, Y.5
Vunnam, S.6
Odingo, J.7
Pu, H.8
Nakanishi, K.9
Berova, N.10
Liotta, D.11
Bielawska, A.12
Hannun, Y.13
-
18
-
-
85030293740
-
-
note
-
(b) The amplitudes of CD spectra shown in Figure 6 should be taken as more authentic in the few cases where minor differences are noted with those reported in ref 10a.
-
-
-
-
21
-
-
33748238501
-
-
12. Ikemoto, N.; Lo, L.-Ch.; Nakanishi, K. Angew. Chem. Int. Ed. Engl. 1992, 31, 890.
-
(1992)
Angew. Chem. Int. Ed. Engl.
, vol.31
, pp. 890
-
-
Ikemoto, N.1
Lo, L.-Ch.2
Nakanishi, K.3
-
22
-
-
85030291330
-
-
note
-
13. The yield of this imidation step was improved when anhydrous pyridine and sublimed 2,3-naphthalenedicarboxylic acid anhydride were used.
-
-
-
-
23
-
-
0021066118
-
-
14. Jungalwala, F. B.; Evans, J. E.; Bremer, E.; McCluer, R. H. J. Lipid. Res. 1983, 24, 1380.
-
(1983)
J. Lipid. Res.
, vol.24
, pp. 1380
-
-
Jungalwala, F.B.1
Evans, J.E.2
Bremer, E.3
McCluer, R.H.4
-
24
-
-
0003579674
-
-
Schulman, S. G., Ed.; Wiley-Interscience: New York
-
15. (a) Hulshoff, A.; Lingeman, H. In Molecular Luminescence Spectroscopy, Methods and Applications; Schulman, S. G., Ed.; Wiley-Interscience: New York, 1985; Part 1, pp 621-715;
-
(1985)
Molecular Luminescence Spectroscopy, Methods and Applications
, Issue.PART 1
, pp. 621-715
-
-
Hulshoff, A.1
Lingeman, H.2
-
25
-
-
0023951016
-
-
(b) The first HPLC analysis of fluorescent O-phthalaldehyde derivatives of sphingosine bases has been reported in the following paper. Merrill, Jr, A. H.; Wang, E.; Mullins, R. E.; Jamison, W. C. L.; Nimkar, S.; Liotta, D. C. Anal. Biochem. 1988, 171, 373.
-
(1988)
Anal. Biochem.
, vol.171
, pp. 373
-
-
Merrill A.H., Jr.1
Wang, E.2
Mullins, R.E.3
Jamison, W.C.L.4
Nimkar, S.5
Liotta, D.C.6
-
26
-
-
0024841826
-
-
16. Shibuya, H.; Kawashima, K.; Ikeda, M.; Kitagawa, I. Tetrahedron Lett. 1989, 30, 7205.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 7205
-
-
Shibuya, H.1
Kawashima, K.2
Ikeda, M.3
Kitagawa, I.4
-
27
-
-
0026776987
-
-
17. Shibuya, H.; Kawashima, K.; Narita, N.; Ikeda, M.; Kitagawa, I. Chem. Pharm. Bull. 1992, 40, 1154.
-
(1992)
Chem. Pharm. Bull.
, vol.40
, pp. 1154
-
-
Shibuya, H.1
Kawashima, K.2
Narita, N.3
Ikeda, M.4
Kitagawa, I.5
-
28
-
-
85030297162
-
-
note
-
18. For catalogs of commercial sphingosines: Biomol, 5166 Campus Drive, Plymouth Meeting, PA 19462, U.S.A.; Matreya, Inc., 500 Tressler Street, Pleasant Gap, PA 16823, U.S.A.; Serdary Research Laboratories Inc., 1643 Kathryn Drive, London, Ontario, N6G 2R7, Canada; Sigma, P.O. Box 14508, St. Louis, MO 63178, U.S.A.
-
-
-
-
29
-
-
85030300139
-
-
note
-
19. It should be noted that the fluorescence intensity of N-naphthimido-sphingosines (1C and 2C) is approximately half that of the dihydro series (1c and 2c) in the normal phase HPLC solvent system (data not shown); this should be taken into account in cases where fluorescence intensities are used in estimating the composition ratio.
-
-
-
-
30
-
-
0345897572
-
-
John Wiley: New York
-
20. Organic Synthesis; John Wiley: New York, 1941; Vol. 1, pp 410-411.
-
(1941)
Organic Synthesis
, vol.1
, pp. 410-411
-
-
|