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7
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0028214844
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Nakagawa, T.; Ueno, K.; Kashiwa, M.; Watanabe, J. Tetrahedron Lett. 1994, 35, 1921-1924.
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Nakagawa, T.1
Ueno, K.2
Kashiwa, M.3
Watanabe, J.4
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9
-
-
84894519158
-
-
These references also contain a uniform nomenclature of cyclic oligosaccharides
-
(b) Immel, S.; Brickmann, J.; Lichtenthaler, F. W. Liebigs Ann. 1995, 929-942. These references also contain a uniform nomenclature of cyclic oligosaccharides.
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(1995)
Liebigs Ann.
, pp. 929-942
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Immel, S.1
Brickmann, J.2
Lichtenthaler, F.W.3
-
10
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-
0343590739
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Houdier, S.; Vottero, P. J. A. Angew. Chem. 1994, 106, 365; Angew. Chem. Int. Ed. Engl. 1994, 33, 355-356.
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(1994)
Angew. Chem.
, vol.106
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Houdier, S.1
Vottero, P.J.A.2
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11
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0000492601
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Houdier, S.; Vottero, P. J. A. Angew. Chem. 1994, 106, 365; Angew. Chem. Int. Ed. Engl. 1994, 33, 355-356.
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(1994)
Angew. Chem. Int. Ed. Engl.
, vol.33
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-
-
-
15
-
-
85030200708
-
-
note
-
C 91.2 (C-1), 76.4 (C-2), 75.6 (C-5), 74.4 (C-3), 68.8 (C-4), 61.0 (C-6).
-
-
-
-
17
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-
49549143786
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-
Excoffier, G.; Gagnaire, D.; Utille, J.-P. Carbohydr. Res. 1975, 39, 368-373.
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Carbohydr. Res.
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Excoffier, G.1
Gagnaire, D.2
Utille, J.-P.3
-
18
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-
0001513404
-
-
(a) Schmidt, R. R.; Michel, J. Angew. Chem. 1980, 92, 763-764; Angew. Chem. Int. Ed. Engl. 1980, 19, 731-732.
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Angew. Chem.
, vol.92
, pp. 763-764
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Schmidt, R.R.1
Michel, J.2
-
19
-
-
84985624827
-
-
(a) Schmidt, R. R.; Michel, J. Angew. Chem. 1980, 92, 763-764; Angew. Chem. Int. Ed. Engl. 1980, 19, 731-732.
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(1980)
Angew. Chem. Int. Ed. Engl.
, vol.19
, pp. 731-732
-
-
-
20
-
-
0023654997
-
-
(b) Numata, M.; Sugimoto, M.; Koike, K.; Ogawa, T. Carbohydr. Res. 1987, 163, 209-225.
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Carbohydr. Res.
, vol.163
, pp. 209-225
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Numata, M.1
Sugimoto, M.2
Koike, K.3
Ogawa, T.4
-
22
-
-
0028034436
-
-
Levy, D. E.; Dasgupta, F.; Tang, P. C. Tetrahedron: Asymmetry 1994, 5, 2265-2268.
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(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 2265-2268
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Levy, D.E.1
Dasgupta, F.2
Tang, P.C.3
-
23
-
-
85030209751
-
-
note
-
Atom numbering is defined in Ref. 11.
-
-
-
-
24
-
-
85030203420
-
-
note
-
This compound was obtained from 3 by successive hydrogenolysis, acetylation, followed by conversions b and c in Scheme 1.
-
-
-
-
26
-
-
0001387149
-
-
Jeffrey, G. A.; McMullan, R. K.; Takagi, S. Acta Crystallographica 1977, B33, 728-737.
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(1977)
Acta Crystallographica
, vol.B33
, pp. 728-737
-
-
Jeffrey, G.A.1
McMullan, R.K.2
Takagi, S.3
-
28
-
-
85030207217
-
-
note
-
The exo-anomeric effect would require this angle to be ca. -60°. In methyl α-D-glucopyranoside the corresponding angle is, indeed, -54.4° (Ref. 20).
-
-
-
-
29
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0026414072
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-
For a discussion of the stabilizing factors in a related tricyclic saccharide harboring a flexible dioxane moiety, see: Bock, K.; Pedersen, C.; Defaye, J.; Gadelle, A. K. Carbohydr. Res. 1991, 216, 141-148.
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Carbohydr. Res.
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-
Bock, K.1
Pedersen, C.2
Defaye, J.3
Gadelle, A.K.4
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