Highly Stereoselective Synthesis of 1,2-trans-Glycosides Using p-Chlorobenzylated Glycosyl Carbonate as Glycosyl Donor

Teruaki Mukaiyama; Kazuo Miyazaki; Hiromi Uchiro

doi:10.1246/cl.1998.635

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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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Stereoselective Synthesis (Part K)

10.1016/s1572-5995(06)x8144-9 ◽

1995 ◽

Keyword(s):

Stereoselective Synthesis

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