-
1
-
-
0000288777
-
Total synthesis of allosamidin: An application of the sulfonamidoglycosylation of glycals
-
Griffith, D.; Danishefsky, S. Total synthesis of allosamidin: an application of the sulfonamidoglycosylation of glycals. J. Am. Chem. Soc. 1991, 113, 5863-5864.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 5863-5864
-
-
Griffith, D.1
Danishefsky, S.2
-
2
-
-
0033010841
-
Chemistry and biology of trehazolins
-
Kobayashi, Y. Chemistry and biology of trehazolins. Carbohydr. Res. 1999, 315, 3-15.
-
(1999)
Carbohydr. Res.
, vol.315
, pp. 3-15
-
-
Kobayashi, Y.1
-
3
-
-
84989580263
-
Mimicking the glucosidase transition state: Shape/charge considerations
-
Ganem, B.; Papandreou, G. Mimicking the glucosidase transition state: shape/charge considerations. J. Am. Chem. Soc. 1991, 113, 8984-8985.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 8984-8985
-
-
Ganem, B.1
Papandreou, G.2
-
4
-
-
0030838247
-
Discovery of methyl-2-(2′-hydroxyphenyl)-2-oxazoline-4-carboxylate as a secondary metabolite from actinomadura
-
Sasaki, T.; Otani, T.; Yoshida, K.; Unemi, N.; Hamada, M.; Takeuchi, T. Discovery of methyl-2-(2′-hydroxyphenyl)-2-oxazoline-4-carboxylate as a secondary metabolite from actinomadura. J. Antibiotics 1997, 50 (10), 881-883.
-
(1997)
J. Antibiotics
, vol.50
, Issue.10
, pp. 881-883
-
-
Sasaki, T.1
Otani, T.2
Yoshida, K.3
Unemi, N.4
Hamada, M.5
Takeuchi, T.6
-
6
-
-
27744438896
-
Synthetic and conformational aspects of trimethylammonium-methyl substituted 2-oxazolines as potential cholinergics
-
Fotador, U.; Becu, C.; Borremans, F.; Anteunis, M. Synthetic and conformational aspects of trimethylammonium-methyl substituted 2-oxazolines as potential cholinergics. Tetrahedron 1978, 34, 3537-3544.
-
(1978)
Tetrahedron
, vol.34
, pp. 3537-3544
-
-
Fotador, U.1
Becu, C.2
Borremans, F.3
Anteunis, M.4
-
7
-
-
0026285756
-
COR3224 - A new antidepressant: Pharmacokinetics and metabolism in rat
-
Neau, B.; Damaj, I.; Lambrey, B.; Akbaraly, J.; Roux, J.; Perrissoud, D.; Jacquot, J. COR3224 - a new antidepressant: pharmacokinetics and metabolism in rat. Eur. J. Drug Metab. Pharmacokinet. 1991, Spec No 3: 77-79.
-
(1991)
Eur. J. Drug Metab. Pharmacokinet.
, Issue.3 SPEC NO
, pp. 77-79
-
-
Neau, B.1
Damaj, I.2
Lambrey, B.3
Akbaraly, J.4
Roux, J.5
Perrissoud, D.6
Jacquot, J.7
-
8
-
-
0028037899
-
Human rhinovirus 14 complexed with fragments of active antiviral compounds
-
Bibler-Muckelbauer, J.; Kremer, M.; Rossmann, M.; Diana, G.; Dutko, F.; Pevear, D.; McKinlay, M. Human rhinovirus 14 complexed with fragments of active antiviral compounds. Virology 1994, 202, 360-369.
-
(1994)
Virology
, vol.202
, pp. 360-369
-
-
Bibler-Muckelbauer, J.1
Kremer, M.2
Rossmann, M.3
Diana, G.4
Dutko, F.5
Pevear, D.6
McKinlay, M.7
-
9
-
-
33847801270
-
Halide ion catalyzed glycosidation reactions. Syntheses of α-linked disaccharides
-
Lemieux, R.U.; Hendriks, K.B.; Stick, R.V.; James, K. Halide ion catalyzed glycosidation reactions. Syntheses of α-linked disaccharides. J. Am. Chem. Soc. 1975, 97, 4056-4062.
-
(1975)
J. Am. Chem. Soc.
, vol.97
, pp. 4056-4062
-
-
Lemieux, R.U.1
Hendriks, K.B.2
Stick, R.V.3
James, K.4
-
10
-
-
84989568635
-
Synthese α-verknupfter-2′-deoxy-2-iododisaccharide
-
Thiem, J.; Karl, H.; Schwenter, J. Synthese α-verknupfter-2′- deoxy-2-iododisaccharide. Synthesis 1978, 696.
-
(1978)
Synthesis
, pp. 696
-
-
Thiem, J.1
Karl, H.2
Schwenter, J.3
-
11
-
-
84913962444
-
Highly selective synthesis of α-L-olivomycosides via trimethylsilyl triflate mediated glycosidations of 1-O-acetyl-4-O-isobutyrl-2,6-dideoxy-2- iodo-3-C-methyl-α-L-mannopyranose
-
Roush, W.; Briner, K.; Sebesta, D. Highly selective synthesis of α-L-olivomycosides via trimethylsilyl triflate mediated glycosidations of 1-O-acetyl-4-O-isobutyrl-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranose. Synlett 1993, 264-265.
-
(1993)
Synlett
, pp. 264-265
-
-
Roush, W.1
Briner, K.2
Sebesta, D.3
-
12
-
-
84986703456
-
Synthese von 2-desoxy-α-O-glycopeptiden mit dem N-Iodsuccinimid-(NIS-) Verfahren
-
Kottenhahn, M.; Kessler, H. Synthese von 2-desoxy-α-O-glycopeptiden mit dem N-Iodsuccinimid-(NIS-) Verfahren. Liebigs Ann. Chem. 1991, 727-744.
-
(1991)
Liebigs Ann. Chem.
, pp. 727-744
-
-
Kottenhahn, M.1
Kessler, H.2
-
13
-
-
0001465658
-
Stereoselectivity in glucal epoxide formation
-
Marzabadi, C.; Spilling, C.D. Stereoselectivity in glucal epoxide formation. J. Org. Chem. 1993, 58, 3761-3766.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 3761-3766
-
-
Marzabadi, C.1
Spilling, C.D.2
-
14
-
-
0347991622
-
Reactivity of 2-deoxy-2-iodoglycosyl isothiocyanates with O-, S-, and N- Nucleophiles, synthesis of glycopyranoso-fused thiazoles
-
Isac-Garcia, J.; Hernandez-Mateo, F.; Calvo-Flores, F.; Santoyo-Gonzalez, F. Reactivity of 2-deoxy-2-iodoglycosyl isothiocyanates with O-, S-, and N- nucleophiles, synthesis of glycopyranoso-fused thiazoles. J. Org. Chem. 2004, 69, 202-205.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 202-205
-
-
Isac-Garcia, J.1
Hernandez-Mateo, F.2
Calvo-Flores, F.3
Santoyo-Gonzalez, F.4
-
15
-
-
0000360619
-
Sulfonamidoglycosylation of glycals. A route to oligosaccharides with 2-aminohexose subunits
-
Griffith, D.; Danishefsky, S. Sulfonamidoglycosylation of glycals. A route to oligosaccharides with 2-aminohexose subunits. J. Am. Chem. Soc. 1990, 112, 5811-5819.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 5811-5819
-
-
Griffith, D.1
Danishefsky, S.2
-
16
-
-
4143104580
-
The preparation of 2-iodoamides from glucals and their further transformations into oxazolines
-
De Castro, M.; Marzabadi, C. The preparation of 2-iodoamides from glucals and their further transformations into oxazolines. Tetrahedron Lett. 2004, 45, 6501-6504.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 6501-6504
-
-
De Castro, M.1
Marzabadi, C.2
-
17
-
-
0000889719
-
Syntheses of deoxy oligosaccharides
-
Thiem, J., Ed.; Springer-Verlag: Berlin
-
Thiem, J.; Klatke, W. Syntheses of deoxy oligosaccharides. In Topics in Current Chemistry, Carbohydrate Chemistry; Thiem, J., Ed.; Springer-Verlag: Berlin, 1990; Vol. 154, 285-330.
-
(1990)
Topics in Current Chemistry, Carbohydrate Chemistry
, vol.154
, pp. 285-330
-
-
Thiem, J.1
Klatke, W.2
-
18
-
-
27844586676
-
Furans: Reactions and synthesis
-
Blackwell Science: Oxford
-
Furan is generally considered the "least aromatic" of the five-membered ring heterocycles containing only a single heteroatom and has a greater tendency to react to give addition products. See Joule, J.; Mills, K. Furans: reactions and synthesis. In Heterocyclic Chemistry, 4th Edition; Blackwell Science: Oxford, 2000; 296-318.
-
(2000)
Heterocyclic Chemistry, 4th Edition
, pp. 296-318
-
-
Joule, J.1
Mills, K.2
-
19
-
-
0001365410
-
Ritter-like reactions of 1,2- Anhydropyranose derivatives
-
(a) Gordon, D.M.; Danishefsky, S.J. Ritter-like reactions of 1,2- anhydropyranose derivatives. J. Org. Chem. 1991, 56, 3713-3715;
-
(1991)
J. Org. Chem.
, vol.56
, pp. 3713-3715
-
-
Gordon, D.M.1
Danishefsky, S.J.2
-
20
-
-
0037151559
-
C2-Amidoglycosylation. Scope and mechanism of nitrogen transfer
-
(b) Liu, J.; Gin, D. C2-Amidoglycosylation. Scope and mechanism of nitrogen transfer. J. Am. Chem. Soc. 2002, 124, 9789-9797.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 9789-9797
-
-
Liu, J.1
Gin, D.2
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