Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Hisashi Maeshima"'
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A Catalytic and Stereoselective Glycosylation withβ-Glycosyl Fluorides
Autor: Kazuya Takeuchi, Hisashi Maeshima, Terunobu Saitoh, Teruaki Mukaiyama, Hideki Jona
Publikováno v: Helvetica Chimica Acta. 83:1901-1918
A catalytic and stereoselective glycosylation of several glycosyl acceptors with β-D-glycosyl fluoride was successfully performed in the presence of a catalytic amount of trityl tetrakis(pentafluorophenyl)borate (TrB(C6F5)4) or trifluoromethanesulfo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8318abe800a4721cae81ccc94c8e17c1
https://doi.org/10.1002/1522-2675(20000809)83:8<1901::aid-hlca1901>3.0.co
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3
ChemInform Abstract: Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride by Using a Combination of Stannous(II) Chloride (SnCl2) and Silver Tetrakis(pentafluorophenyl)borate [AgB(C6F5)4] as a Catalyst
Autor: Hisashi Maeshima, Hideki Jona, Teruaki Mukaiyama
Publikováno v: ChemInform. 32
A catalytic and stereoselective glycosylation of various glycosyl acceptors with disarmed glycosyl fluorides is successfully carried out by using a combination of stannous(II) chloride (SnCl2) and silver tetrakis(pentafluorophenyl)borate [AgB(C6F5)4]
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cd9ce4235275236afa98406002198007
https://doi.org/10.1002/chin.200142227
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4
ChemInform Abstract: Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride Having Phthaloyl or Dichlorophthaloyl Protected Amino Function Using a 1:2 Combination of Stannic Chloride and Silver Tetrakis(pentafluorophenyl)borate
Autor: Hideki Jona, Teruaki Mukaiyama, Hisashi Maeshima
Publikováno v: ChemInform. 32
A catalytic and stereoselective glycosylation of various glycosyl acceptors with disarmed glycosyl fluorides having phthaloyl or dichlorophthaloyl protected amino function is successfully carried out by using a combination of stannic chloride (SnCl4)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2814bc1934f92ea5d7cf127bf09d0173
https://doi.org/10.1002/chin.200151192
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6
Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride Having Phthaloyl or Dichlorophthaloyl Protected Amino Function Using a 1 : 2 Combination of Stannic Chloride and Silver Tetrakis(pentafluorophenyl)borate
Autor: Teruaki Mukaiyama, Hideki Jona, Hisashi Maeshima
Publikováno v: Chemistry Letters. 30:726-727
A catalytic and stereoselective glycosylation of various glycosyl acceptors with disarmed glycosyl fluorides having phthaloyl or dichlorophthaloyl protected amino function is successfully carried out by using a combination of stannic chloride (SnCl4)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6a4d36b4bf5e3f30e62971f7d885a37a
https://doi.org/10.1246/cl.2001.726
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7
Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride by Using a Combination of Stannous(II) Chloride (SnCl2) and Silver Tetrakis(pentafluorophenyl)borate [AgB(C6F5)4] as a Catalyst
Autor: Hisashi Maeshima, Teruaki Mukaiyama, Hideki Jona
Publikováno v: Chemistry Letters. 30:388-389
A catalytic and stereoselective glycosylation of various glycosyl acceptors with disarmed glycosyl fluorides is successfully carried out by using a combination of stannous(II) chloride (SnCl2) and silver tetrakis(pentafluorophenyl)borate [AgB(C6F5)4]
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4ee0e97fcd8af39ec721030aa514c1a3
https://doi.org/10.1246/cl.2001.388
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