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Highly Stereoselective Synthesis of 1,2-trans-Glycosides Using p-Chlorobenzylated Glycosyl Carbonate as Glycosyl Donor
Chemistry Letters
◽
10.1246/cl.1998.635
◽
1998
◽
Vol 27
(7)
◽
pp. 635-636
◽
Cited By ~ 16
Author(s):
Teruaki Mukaiyama
◽
Kazuo Miyazaki
◽
Hiromi Uchiro
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
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Cited By
References
ChemInform Abstract: Highly Stereoselective Synthesis of 1,2-trans-Glycosides Using p-Chlorobenzylated Glycosyl Carbonate as Glycosyl Donor.
ChemInform
◽
10.1002/chin.199848231
◽
2010
◽
Vol 29
(48)
◽
pp. no-no
Author(s):
T. MUKAIYAMA
◽
K. MIYAZAKI
◽
H. UCHIRO
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
Stereoselective synthesis of α-L-Fucp-(1,2)- and -(1,3)-β-D-Galp(1)-4-methylumbelliferone using glycosyl donor substituted by propane-1,3-diyl phosphate as leaving group
Journal of the Chemical Society Perkin Transactions 1
◽
10.1039/b002754p
◽
2000
◽
pp. 2187-2193
◽
Cited By ~ 9
Author(s):
Hariprasad Vankayalapati
◽
Gurdial Singh
Keyword(s):
Stereoselective Synthesis
◽
Leaving Group
◽
Glycosyl Donor
Download Full-text
Stereoselective Synthesis of 2-C-Acetonyl-2-Deoxy-d-Galactosides using 1,2-Cyclopropaneacetylated Sugar as Novel Glycosyl Donor
Organic Letters
◽
10.1021/ol902732w
◽
2010
◽
Vol 12
(3)
◽
pp. 540-543
◽
Cited By ~ 22
Author(s):
Qiang Tian
◽
Liyan Xu
◽
Xiaofeng Ma
◽
Wei Zou
◽
Huawu Shao
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
Phenyl 2-azido-2-deoxy-1-selenogalactosides: a single type of glycosyl donor for the highly stereoselective synthesis of α- and β-2-azido-2-deoxy-d-galactopyranosides
Tetrahedron Letters
◽
10.1016/j.tetlet.2016.01.013
◽
2016
◽
Vol 57
(6)
◽
pp. 708-711
◽
Cited By ~ 8
Author(s):
Elena A. Khatuntseva
◽
Andrey A. Sherman
◽
Yury E. Tsvetkov
◽
Nikolay E. Nifantiev
Keyword(s):
Stereoselective Synthesis
◽
Single Type
◽
Glycosyl Donor
Download Full-text
ChemInform Abstract: Stereoselective Synthesis of α-L-Fucp-(1,2)- and -(1,3)-β-D-Galp(1)-4-methylumbelliferone Using Glycosyl Donor Substituted by Propane-1,3-diyl Phosphate as Leaving Group.
ChemInform
◽
10.1002/chin.200045215
◽
2000
◽
Vol 31
(45)
◽
pp. no-no
Author(s):
Hariprasad Vankayalapati
◽
Gurdial Singh
Keyword(s):
Stereoselective Synthesis
◽
Leaving Group
◽
Glycosyl Donor
Download Full-text
Catalytic Stereoselective Synthesis of α- or β-Glucosides Using a Single Glycosyl Donor, 1-O-2′-(2′-Methoxyethoxy)acetyl-Glucopyranose Derivative
Chemistry Letters
◽
10.1246/cl.1993.1373
◽
1993
◽
Vol 22
(8)
◽
pp. 1373-1376
◽
Cited By ~ 15
Author(s):
Koki Matsubara
◽
Takenori Sasaki
◽
Teruaki Mukaiyama
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
ChemInform Abstract: Stereoselective Synthesis of 2-C-Acetonyl-2-deoxy-D-galactosides Using 1,2-Cyclopropaneacetylated Sugar as Novel Glycosyl Donor.
ChemInform
◽
10.1002/chin.201026191
◽
2010
◽
Vol 41
(26)
◽
pp. no-no
Author(s):
Qiang Tian
◽
Liyan Xu
◽
Xiaofeng Ma
◽
Wei Zou
◽
Huawu Shao
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
ChemInform Abstract: Methodology for the Stereoselective Synthesis of Nucleosides Utilizing 1-Thioglycoside as Glycosyl Donor
ChemInform
◽
10.1002/chin.199923321
◽
2010
◽
Vol 30
(23)
◽
pp. no-no
Author(s):
Hideyuki Sugimura
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
ChemInform Abstract: Catalytic Stereoselective Synthesis of α- or β-Glucosides Using a Single Glycosyl Donor, 1-O-2′-(2′-Methoxyethoxy) acetylglucopyranose Derivative.
ChemInform
◽
10.1002/chin.199401283
◽
2010
◽
Vol 25
(1)
◽
pp. no-no
Author(s):
K. MATSUBARA
◽
T. SASAKI
◽
T. MUKAIYAMA
Keyword(s):
Stereoselective Synthesis
◽
Glycosyl Donor
Download Full-text
Stereoselective Synthesis (Part K)
10.1016/s1572-5995(06)x8144-9
◽
1995
◽
Keyword(s):
Stereoselective Synthesis
Download Full-text
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