-
1
-
-
0037049166
-
Stereoselective synthesis of D-erythro- and L-threo-sphinganines via palladium-catalyzed equilibration and Suzuki coupling
-
Cook, G. R. and Pararajasingham, K., Stereoselective synthesis of D-erythro- and L-threo-sphinganines via palladium-catalyzed equilibration and Suzuki coupling. Tetrahedron Letters, 43, 9027-9029 (2002).
-
(2002)
Tetrahedron Letters
, vol.43
, pp. 9027-9029
-
-
Cook, G.R.1
Pararajasingham, K.2
-
2
-
-
0029883037
-
Aziridine-2-carboxylic acid mediated asymmetric synthesis of D-erythro and L-threo-sphingosine from a common precursor
-
Davis, F. A. and Reddy, G. V., Aziridine-2-carboxylic acid mediated asymmetric synthesis of D-erythro and L-threo-sphingosine from a common precursor. Tetrahedron Letters, 37, 25, 4349-4352 (1996).
-
(1996)
Tetrahedron Letters
, vol.37
, Issue.25
, pp. 4349-4352
-
-
Davis, F.A.1
Reddy, G.V.2
-
3
-
-
0023684709
-
A Stereodivergent synthesis of D-erythro-sphingosine and D-threo-sphingosine from L-serine
-
Garner, P., Park, J. M., and Malecki, E., A Stereodivergent synthesis of D-erythro-sphingosine and D-threo-sphingosine from L-serine. J. Org. Chem., 53, 4395-4398 (1988).
-
(1988)
J. Org. Chem
, vol.53
, pp. 4395-4398
-
-
Garner, P.1
Park, J.M.2
Malecki, E.3
-
4
-
-
0022974603
-
Sphingosine inhibition of protein kinase C activity and of phorbol dibutyrate binding in vitro and in human platelets
-
Hannun, Y. A., Loomis, C. R., Merrill, A. H. Jr., and Bell, R. M., Sphingosine inhibition of protein kinase C activity and of phorbol dibutyrate binding in vitro and in human platelets. J. Biol. Chem., 261, 12604-12609 (1986).
-
(1986)
J. Biol. Chem
, vol.261
, pp. 12604-12609
-
-
Hannun, Y.A.1
Loomis, C.R.2
Merrill Jr., A.H.3
Bell, R.M.4
-
6
-
-
0042092145
-
Chirospecific synthesis of D-erythro- and L-threo-sphinganines from sugars
-
Jeong, I. Y., Lee, J. H., Lee, B. W., Kim, J. H., and Park, K. H., Chirospecific synthesis of D-erythro- and L-threo-sphinganines from sugars. Bull. Korean Chem. Soc., 24, 5, 617-622 (2003).
-
(2003)
Bull. Korean Chem. Soc
, vol.24
, Issue.5
, pp. 617-622
-
-
Jeong, I.Y.1
Lee, J.H.2
Lee, B.W.3
Kim, J.H.4
Park, K.H.5
-
7
-
-
0000234680
-
Highly diastereoselective synthesis of D-threo- and D-erythro-sphingosine from glycidol
-
Katsumura, S., Yamamoto, N., Fukuda, E., and Iwama, S., Highly diastereoselective synthesis of D-threo- and D-erythro-sphingosine from glycidol. Chemistry letters, 393 (1995).
-
(1995)
Chemistry letters
, vol.393
-
-
Katsumura, S.1
Yamamoto, N.2
Fukuda, E.3
Iwama, S.4
-
8
-
-
0037155732
-
A short and efficient stereoselective synthesis of all four diastereomers of sphingosine
-
Lee, J. M., Lim, H. S., and Chung, S. K., A short and efficient stereoselective synthesis of all four diastereomers of sphingosine. Tetrahedron: Asymmetry, 13, 343-347 (2002).
-
(2002)
Tetrahedron: Asymmetry
, vol.13
, pp. 343-347
-
-
Lee, J.M.1
Lim, H.S.2
Chung, S.K.3
-
9
-
-
0034649736
-
Facile and efficient total synthesis of (+)-preussin
-
Lee, K. Y., Kim, Y. H., Oh, C. Y., and Ham, W. H., Facile and efficient total synthesis of (+)-preussin. Org. Lett., 2, 25, 4041-4042 (2000).
-
(2000)
Org. Lett
, vol.2
, Issue.25
, pp. 4041-4042
-
-
Lee, K.Y.1
Kim, Y.H.2
Oh, C.Y.3
Ham, W.H.4
-
10
-
-
0032578739
-
A highly stereocontrolled asymmetric synthesis of the taxol C-13 side chain; (4S, 5R)-2,4-Diphenyloxazoline-5-carboxylic acid
-
Lee, K. Y., Kim, Y. H., Park, M. S., and Ham, W. H., A highly stereocontrolled asymmetric synthesis of the taxol C-13 side chain; (4S, 5R)-2,4-Diphenyloxazoline-5-carboxylic acid. Tetrahedron letters, 39, 8129-8132 (1998).
-
(1998)
Tetrahedron letters
, vol.39
, pp. 8129-8132
-
-
Lee, K.Y.1
Kim, Y.H.2
Park, M.S.3
Ham, W.H.4
-
11
-
-
0033601212
-
Stereoselective intramolecular cyclization of allyl and homoallyl benzamide via ?-allylpalladium complex catalyzed by Pd(0)
-
Lee, K. Y., Kim, Y. H., Park, M. S., Oh, C. Y., and Ham, W. H., Stereoselective intramolecular cyclization of allyl and homoallyl benzamide via ?-allylpalladium complex catalyzed by Pd(0). J. Org. Chem., 64, 9450-9458 (1999).
-
(1999)
J. Org. Chem
, vol.64
, pp. 9450-9458
-
-
Lee, K.Y.1
Kim, Y.H.2
Park, M.S.3
Oh, C.Y.4
Ham, W.H.5
-
12
-
-
0037069722
-
Total synthesis of sphingofungin F
-
Lee, K. Y., Oh, C. Y., and Ham, W. H., Total synthesis of sphingofungin F. Org. Lett., 4, 25, 4403-4405 (2002a).
-
(2002)
Org. Lett
, vol.4
, Issue.25
, pp. 4403-4405
-
-
Lee, K.Y.1
Oh, C.Y.2
Ham, W.H.3
-
13
-
-
0037121588
-
Total synthesis of myriocin
-
Lee, K. Y., Oh, C. Y., Kim, Y. H. Joo, J. E., and Ham, W. H., Total synthesis of myriocin. Tetrahedron Letters, 43, 9361-9363 (2002b).
-
(2002)
Tetrahedron Letters
, vol.43
, pp. 9361-9363
-
-
Lee, K.Y.1
Oh, C.Y.2
Kim, Y.H.3
Joo, J.E.4
Ham, W.H.5
-
14
-
-
0037421233
-
Stereoselective synthesis of (+)-spectaline
-
Lee, Y. S., Shin, Y. H., Kim, Y. H., Lee, K. Y., Oh, C. Y., Pyun, S. J., Park, H. J., Jeong, J. H., and Ham, W. H., Stereoselective synthesis of (+)-spectaline. Tetrahedron: Asymmetry, 14, 87-93 (2003).
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 87-93
-
-
Lee, Y.S.1
Shin, Y.H.2
Kim, Y.H.3
Lee, K.Y.4
Oh, C.Y.5
Pyun, S.J.6
Park, H.J.7
Jeong, J.H.8
Ham, W.H.9
-
15
-
-
0032537678
-
Stereoselective synthesis of sphinganine by means of modified asymmetric borane reduction
-
Masuia, M. and Shioiri, T., Stereoselective synthesis of sphinganine by means of modified asymmetric borane reduction. Tetrahedron Letters, 39, 5199-5200 (1998).
-
(1998)
Tetrahedron Letters
, vol.39
, pp. 5199-5200
-
-
Masuia, M.1
Shioiri, T.2
-
16
-
-
0023904902
-
A stereoselective synthesis of sphingosine, a protein kinase C inhibitor
-
Nimkar, S., Menaldino, D., Merrill, A. H., and Liotta, D., A stereoselective synthesis of sphingosine, a protein kinase C inhibitor. Tetrahedron Letters, 29, 25, 3037-3040 (1988).
-
(1988)
Tetrahedron Letters
, vol.29
, Issue.25
, pp. 3037-3040
-
-
Nimkar, S.1
Menaldino, D.2
Merrill, A.H.3
Liotta, D.4
-
17
-
-
0037459676
-
Divergent synthesis of D-erythro-sphingosine, L-threo-sphingosine, and their regioisomers
-
Olofsson, B. and Somfai, P. Divergent synthesis of D-erythro-sphingosine, L-threo-sphingosine, and their regioisomers. J. Org. Chem., 68, 2514-2517 (2003).
-
(2003)
J. Org. Chem
, vol.68
, pp. 2514-2517
-
-
Olofsson, B.1
Somfai, P.2
-
18
-
-
0026730481
-
Aluminoxy acetals from α-amino esters: Chirality transfer via sequential addition of hydride and C-nucleophiles. 2-amino alcohols and sphingosines
-
Polt, R., Peterson, M. A., and Young, L. D., Aluminoxy acetals from α-amino esters: chirality transfer via sequential addition of hydride and C-nucleophiles. 2-amino alcohols and sphingosines. J. Org. Chem., 57, 5469-5480 (1992).
-
(1992)
J. Org. Chem
, vol.57
, pp. 5469-5480
-
-
Polt, R.1
Peterson, M.A.2
Young, L.D.3
-
19
-
-
0347720706
-
Synthesis of (+)-1-deoxygalactonojirimycin
-
Pyun, S. J., Lee, K. Y., Oh, C. Y., and Ham, W. H., Synthesis of (+)-1-deoxygalactonojirimycin. Heterocycles, 62, 333-341 (2004).
-
(2004)
Heterocycles
, vol.62
, pp. 333-341
-
-
Pyun, S.J.1
Lee, K.Y.2
Oh, C.Y.3
Ham, W.H.4
-
20
-
-
12344251818
-
Total synthesis of 1-deoxygulonojirimycin. revision of the absolute configuration of the natural product
-
Pyun, S. J., Lee, K. Y., Oh, C. Y., Joo, J. E., Cheon, S. H., and Ham, W. H., Total synthesis of 1-deoxygulonojirimycin. revision of the absolute configuration of the natural product. Tetrahedron, 61, 1413-1416 (2005).
-
(2005)
Tetrahedron
, vol.61
, pp. 1413-1416
-
-
Pyun, S.J.1
Lee, K.Y.2
Oh, C.Y.3
Joo, J.E.4
Cheon, S.H.5
Ham, W.H.6
-
21
-
-
0028875444
-
Efficient diastereoselective and enantioselective nitroaldol reactions from prochiral starting materials: Utilization of La-Li-6,6′- disubstituted BINOL complexes as asymmetric catalysts
-
Sasai, H., Tokunaga, T., Watanabe, S., Suzuki, T. Itoh, N., and Shibasaki, M., Efficient diastereoselective and enantioselective nitroaldol reactions from prochiral starting materials: utilization of La-Li-6,6′- disubstituted BINOL complexes as asymmetric catalysts. J. Org. Chem., 60, 7388-7389 (1996).
-
(1996)
J. Org. Chem
, vol.60
, pp. 7388-7389
-
-
Sasai, H.1
Tokunaga, T.2
Watanabe, S.3
Suzuki, T.4
Itoh, N.5
Shibasaki, M.6
-
22
-
-
33845666640
-
An asymmetric synthesis of (2S,3S)-safingol
-
Sharma, A., Gamre, S., and Chattopadhyay, S., An asymmetric synthesis of (2S,3S)-safingol. Tetrahedron Letters, 48, 633-634 (2007).
-
(2007)
Tetrahedron Letters
, vol.48
, pp. 633-634
-
-
Sharma, A.1
Gamre, S.2
Chattopadhyay, S.3
-
23
-
-
0024841826
-
18-sphingosines
-
18-sphingosines. Tetrahedron Letters, 30, 51, 7205-7208 (1989).
-
(1989)
Tetrahedron Letters
, vol.30
, Issue.51
, pp. 7205-7208
-
-
Shibuya, H.1
Kawashima, K.2
Ikeda, M.3
Kitagawa, L.4
-
24
-
-
0025911978
-
18-sphingosines via the anomalous version of the Katsuki-Sharpless asymmetric epoxidation reaction
-
18-sphingosines via the anomalous version of the Katsuki-Sharpless asymmetric epoxidation reaction. J. Chem. Soc., Chem. Commun., 820-821 (1991).
-
(1991)
J. Chem. Soc., Chem. Commun
, vol.820-821
-
-
Takano, S.1
Lwabuchi, Y.2
Ogasawara, K.3
-
25
-
-
0343462456
-
Enantiopure aminotriol from D-isoascorbic acid synthesis of D-threo-C-18-sphingosine
-
Tuch, A., Saniere, M. Merrer Y. L., and Depezay, J. C., Enantiopure aminotriol from D-isoascorbic acid synthesis of D-threo-C-18-sphingosine. Tetrahedron: Asymmetry, 7, 897-906 (1996).
-
(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 897-906
-
-
Tuch, A.1
Saniere, M.2
Merrer, Y.L.3
Depezay, J.C.4
-
26
-
-
11844294912
-
Asymmetric synthesis of (+)-L-733,060
-
Yoon, Y. J., Joo, J. E., Lee, K. Y., Kim, Y. H., Oh, C. Y., and Ham, W. H., Asymmetric synthesis of (+)-L-733,060. Tetrahedron Letters, 46, 739-741 (2005).
-
(2005)
Tetrahedron Letters
, vol.46
, pp. 739-741
-
-
Yoon, Y.J.1
Joo, J.E.2
Lee, K.Y.3
Kim, Y.H.4
Oh, C.Y.5
Ham, W.H.6
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