-
1
-
-
0002614201
-
-
Khan, S.H, O'Neill, R.A, Eds, Harwood Academic: New York
-
(a) Grindley, T.B. In Modern Methods in Carbohydrate Synthesis; Khan, S.H., O'Neill, R.A., Eds.; Harwood Academic: New York, 1996; 225-250;
-
(1996)
In Modern Methods in Carbohydrate Synthesis
, pp. 225-250
-
-
Grindley, T.B.1
-
4
-
-
0034622080
-
Concise syntheses of L-a-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP), 5-phosphate (5-PIP), and 3,5-bisphosphate (3,5-PIP2)
-
For examples, see: a
-
For examples, see: (a) Falck, J.R.; Muralikrishna, U.; Katipally, K.R.; Capdevila, J.H.; Ulug, E.T. Concise syntheses of L-a-phosphatidyl-D-myo-inositol 3-phosphate (3-PIP), 5-phosphate (5-PIP), and 3,5-bisphosphate (3,5-PIP2). Tetrahedron Lett. 2000, 41, 4271-4275;
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 4271-4275
-
-
Falck, J.R.1
Muralikrishna, U.2
Katipally, K.R.3
Capdevila, J.H.4
Ulug, E.T.5
-
5
-
-
0000143204
-
General synthesis of 3-phosphorylated myo-inositol phospholipids and derivatives
-
(b) Painter, G.F.; Groove, S.J.A.; Gilbert, I.H.; Holmes, A.B.; Raithby, P.R.; Hill, M.L.; Hawkins, P.J.; Stephens, L.R. General synthesis of 3-phosphorylated myo-inositol phospholipids and derivatives. J. Chem. Soc., Perkin Trans. 11999, 8, 923-936;
-
(1999)
J. Chem. Soc., Perkin Trans
, vol.1
, Issue.8
, pp. 923-936
-
-
Painter, G.F.1
Groove, S.J.A.2
Gilbert, I.H.3
Holmes, A.B.4
Raithby, P.R.5
Hill, M.L.6
Hawkins, P.J.7
Stephens, L.R.8
-
6
-
-
0000804001
-
-
Biamonte, M.A.; Vasella, A. An advantageous synthesis of ID- and 1L-1,2,3,5/4-cyclohexanepentol. Helv. Chim. Acta 1998, 81, 688-694;
-
(c) Biamonte, M.A.; Vasella, A. An advantageous synthesis of ID- and 1L-1,2,3,5/4-cyclohexanepentol. Helv. Chim. Acta 1998, 81, 688-694;
-
-
-
-
7
-
-
0032029786
-
Racemic 2,4-di-O-benzoyl-myoinositol 1,3,5-orthoformate: A versatile intermediate for the preparation of myoinositol phosphates
-
(d) Das, T.; Shashidhar, M.S. Racemic 2,4-di-O-benzoyl-myoinositol 1,3,5-orthoformate: a versatile intermediate for the preparation of myoinositol phosphates. Carbohydr. Res. 1998, 308, 165-168.
-
(1998)
Carbohydr. Res
, vol.308
, pp. 165-168
-
-
Das, T.1
Shashidhar, M.S.2
-
8
-
-
0034607513
-
Myo-inositol 4,6-carbonate: An easily prepared small molecule with three syn-axial hydroxyl groups
-
(a) Angyal, S.J. Myo-inositol 4,6-carbonate: an easily prepared small molecule with three syn-axial hydroxyl groups. Carbohydr. Res. 2000, 325, 313-320;
-
(2000)
Carbohydr. Res
, vol.325
, pp. 313-320
-
-
Angyal, S.J.1
-
9
-
-
0000678801
-
Synthesis and crystal structure of a unique linear homoditopic ligand bifacially complexed to lithium picrate
-
(b) Paquette, L.A.; Tae, J.; Gallucci, J.C. Synthesis and crystal structure of a unique linear homoditopic ligand bifacially complexed to lithium picrate. Org. Lett. 2000, 2, 143-146;
-
(2000)
Org. Lett
, vol.2
, pp. 143-146
-
-
Paquette, L.A.1
Tae, J.2
Gallucci, J.C.3
-
10
-
-
0000298175
-
Lithium ion-selective binding properties of a conformationally constrained tris(spirotetrahydrofuran) secured to an inositol orthoformate platform
-
(c) Tae, J.; Rogers, R.D.; Paquette, L.A. Lithium ion-selective binding properties of a conformationally constrained tris(spirotetrahydrofuran) secured to an inositol orthoformate platform. Org. Lett. 2000, 2, 139-142;
-
(2000)
Org. Lett
, vol.2
, pp. 139-142
-
-
Tae, J.1
Rogers, R.D.2
Paquette, L.A.3
-
11
-
-
0001737852
-
Chiral analogs of enterobactin with hydrophilic or lipophilic properties
-
(d) Tse, B.; Kishi, Y. Chiral analogs of enterobactin with hydrophilic or lipophilic properties. J. Am. Chem. Soc. 1993, 115, 7892-7893.
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 7892-7893
-
-
Tse, B.1
Kishi, Y.2
-
13
-
-
0029049533
-
Palytoxin analogs from the dinoflagellate Ostreopsis siamensis
-
(b) Usami, M.; Satake, M.; Ishida, S.; Inoue, A.; Kan, Y.; Yasumoto, T. Palytoxin analogs from the dinoflagellate Ostreopsis siamensis. J. Am. Chem. Soc. 1995, 117, 5389-5390;
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 5389-5390
-
-
Usami, M.1
Satake, M.2
Ishida, S.3
Inoue, A.4
Kan, Y.5
Yasumoto, T.6
-
14
-
-
0028577168
-
Synthesis of palytoxin from palytoxin carboxylic acid
-
(c) Suh, E.M.; Kishi, Y. Synthesis of palytoxin from palytoxin carboxylic acid. J. Am. Chem. Soc. 1994, 116, 11205-11206.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 11205-11206
-
-
Suh, E.M.1
Kishi, Y.2
-
15
-
-
0029861709
-
Intervention of carbohydrate recognition by proteins and nucleic acids
-
(a) Sears, P.; Wang, C.-H. Intervention of carbohydrate recognition by proteins and nucleic acids. Proc Natl. Acad. Sci. U. S. A. 1996, 93, 12086-12093;
-
(1996)
Proc Natl. Acad. Sci. U. S. A
, vol.93
, pp. 12086-12093
-
-
Sears, P.1
Wang, C.-H.2
-
16
-
-
0000709078
-
Carbohydrates as drugs and potential therapeutics
-
(b) Witczak, Z.J. Carbohydrates as drugs and potential therapeutics. Curr. Med. Chem. 1995, 1, 392-405.
-
(1995)
Curr. Med. Chem
, vol.1
, pp. 392-405
-
-
Witczak, Z.J.1
-
17
-
-
0032552046
-
-
For leading reviews on C-glycoside synthesis: (a) Du, Y.; Linhardt, R.J.; Vlahov, I.R. Recent advances in stereoselective C-glycoside synthesis. Tetrahedron 1998, 54, 9913-9959;
-
For leading reviews on C-glycoside synthesis: (a) Du, Y.; Linhardt, R.J.; Vlahov, I.R. Recent advances in stereoselective C-glycoside synthesis. Tetrahedron 1998, 54, 9913-9959;
-
-
-
-
18
-
-
0000733916
-
C-Glycosidation technology with free radical reactions
-
(b) Togo, H.; He, W.; Waki, Y.; Yokoyama, M. C-Glycosidation technology with free radical reactions. Synlett 1998, 7, 700-717;
-
(1998)
Synlett
, vol.7
, pp. 700-717
-
-
Togo, H.1
He, W.2
Waki, Y.3
Yokoyama, M.4
-
19
-
-
0033807989
-
Structure of anomeric glycosyl radicals and their transformations under reductive conditions
-
(c) Praly, J.-P. Structure of anomeric glycosyl radicals and their transformations under reductive conditions. Adv. Carbohydr. Chem. Biochem. 2000, 56, 65-151.
-
(2000)
Adv. Carbohydr. Chem. Biochem
, vol.56
, pp. 65-151
-
-
Praly, J.-P.1
-
20
-
-
0034699895
-
A convenient, one-step, synthesis of β-C-glycosidic ketones in aqueous media
-
Rodrigues, F.; Canac, Y.; Lubineau, A. A convenient, one-step, synthesis of β-C-glycosidic ketones in aqueous media. Chem. Commun. 2000, 20, 2049-2050.
-
(2000)
Chem. Commun
, vol.20
, pp. 2049-2050
-
-
Rodrigues, F.1
Canac, Y.2
Lubineau, A.3
-
21
-
-
7044260973
-
-
Liu, F.-W; Liu, H.-M.; Ke, Y.; Zhang, J.-Y. A facile approach to anhydrogalactosucrose derivatives from chlorinated sucrose. Carbohydr. Res. 2004, 339, 2651-2656.
-
Liu, F.-W; Liu, H.-M.; Ke, Y.; Zhang, J.-Y. A facile approach to anhydrogalactosucrose derivatives from chlorinated sucrose. Carbohydr. Res. 2004, 339, 2651-2656.
-
-
-
-
22
-
-
13244259406
-
-
Liu, F.-W; Zhang, Y-B.; Liu, H.-M.; Song, X.-P. Preparation of α and β anomers of 1,2,3,6-tetra-O-acetyl-4-chloro-4-deoxy-D-galactopyranose based upon anomerization and kinetic acetylation. Carbohydr. Res. 2005, 340, 489-495.
-
Liu, F.-W; Zhang, Y-B.; Liu, H.-M.; Song, X.-P. Preparation of α and β anomers of 1,2,3,6-tetra-O-acetyl-4-chloro-4-deoxy-D-galactopyranose based upon anomerization and kinetic acetylation. Carbohydr. Res. 2005, 340, 489-495.
-
-
-
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