A Highly Stereoselective Synthesis of α-Glucosides from 1-O-Acetyl Glucose by Use of Tin(IV) Chloride–Silver Perchlorate Catalyst System

Teruaki Mukaiyama; Tohru Takashima; Manabu Katsurada; Hiroyuki Aizawa

doi:10.1246/cl.1991.533

A Highly Stereoselective Synthesis of α-Glucosides from 1-O-Acetyl Glucose by Use of Tin(IV) Chloride–Silver Perchlorate Catalyst System

Chemistry Letters ◽

10.1246/cl.1991.533 ◽

1991 ◽

Vol 20 (4) ◽

pp. 533-536 ◽

Cited By ~ 37

Author(s):

Teruaki Mukaiyama ◽

Tohru Takashima ◽

Manabu Katsurada ◽

Hiroyuki Aizawa

Keyword(s):

Stereoselective Synthesis ◽

Catalyst System ◽

Silver Perchlorate

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ChemInform Abstract: A Highly Stereoselective Synthesis of α-Glucosides from 1-O- Acetyl Glucose by Use of Tin(IV) Chloride-Silver Perchlorate Catalyst System.

ChemInform ◽

10.1002/chin.199145273 ◽

2010 ◽

Vol 22 (45) ◽

pp. no-no

Author(s):

T. MUKAIYAMA ◽

T. TAKASHIMA ◽

M. KATSURADA ◽

H. AIZAWA

Keyword(s):

Stereoselective Synthesis ◽

Catalyst System ◽

Silver Perchlorate

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A Highly Stereoselective Synthesis of β-Glucosides from Pentaacylglucopyranose and Alkyl Silyl Ether by the Use of a Catalytic Amount of Active Species Generated from Methyltrichlorosilane and Silver Perchlorate

Chemistry Letters ◽

10.1246/cl.1992.2105 ◽

1992 ◽

Vol 21 (11) ◽

pp. 2105-2108 ◽

Cited By ~ 9

Author(s):

Teruaki Mukaiyama ◽

Manabu Katsurada ◽

Yousuke Iida

Keyword(s):

Stereoselective Synthesis ◽

Catalytic Amount ◽

Active Species ◽

Silyl Ether ◽

Silver Perchlorate

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The Catalytic Diels-Alder Reaction Using Combined Catalyst System of Diphenyltin Sulfide or Lawesson’s Reagent and Silver Perchlorate

Chemistry Letters ◽

10.1246/cl.1995.332 ◽

1995 ◽

Vol 24 (4) ◽

pp. 332-332

Keyword(s):

Catalyst System ◽

Alder Reaction ◽

Diels Alder ◽

Lawesson’S Reagent ◽

Diels Alder Reaction ◽

Silver Perchlorate ◽

Lawesson's Reagent

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ChemInform Abstract: The Catalytic Diels-Alder Reaction Using Combined Catalyst System of Diphenyltin Sulfide or Lawesson′s Reagent and Silver Perchlorate.

ChemInform ◽

10.1002/chin.199527065 ◽

2010 ◽

Vol 26 (27) ◽

pp. no-no

Author(s):

T. MUKAIYAMA ◽

K. WATANABE ◽

I. SHIINA

Keyword(s):

Catalyst System ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Silver Perchlorate

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ChemInform Abstract: A Highly Stereoselective Synthesis of β-Glucosides from Pentaacylglucopyranose and Alkyl Silyl Ether by the Use of a Catalytic Amount of Active Species Generated from Methyltrichlorosilane and Silver Perchlorate.

ChemInform ◽

10.1002/chin.199322263 ◽

2010 ◽

Vol 24 (22) ◽

pp. no-no

Author(s):

T. MUKAIYAMA ◽

M. KATSURADA ◽

Y. IIDA

Keyword(s):

Stereoselective Synthesis ◽

Catalytic Amount ◽

Active Species ◽

Silyl Ether ◽

Silver Perchlorate

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The Catalytic Diels-Alder Reaction Using Combined Catalyst System of Diphenyltin Sulfide or Lawesson’s Reagent and Silver Perchlorate

Chemistry Letters ◽

10.1246/cl.1995.1 ◽

1995 ◽

Vol 24 (1) ◽

pp. 1-2 ◽

Cited By ~ 6

Author(s):

Teruaki Mukaiyama ◽

Kimitoshi Watanabe ◽

Isamu Shiina

Keyword(s):

Catalyst System ◽

Alder Reaction ◽

Diels Alder ◽

Lawesson’S Reagent ◽

Diels Alder Reaction ◽

Silver Perchlorate ◽

Lawesson's Reagent

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Stereoselective Synthesis (Part K)

10.1016/s1572-5995(06)x8144-9 ◽

1995 ◽

Keyword(s):

Stereoselective Synthesis

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Catalytic Stereoselective Synthesis of α-Amino Phosphonic Acid Derivatives by Asymmetric Hydrogenation

Synthetic Communications ◽

10.1080/00397919608003678 ◽

1996 ◽

Vol 24 (4) ◽

pp. 777-781 ◽

Cited By ~ 4

Author(s):

Ute Schmidt ◽

Günther Oehme ◽

Hanswalter Krause

Keyword(s):

Phosphonic Acid ◽

Stereoselective Synthesis ◽

Asymmetric Hydrogenation

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Stereoselective Synthesis By Robert S. Atkinson, University of Leicester. John Wiley & Sons, Inc., New York, NY. 1995. xii + 529 pp. 15 × 23 cm. $59.95. ISBN 0-471-954195.

Journal of Natural Products ◽

10.1021/np960463b ◽

1996 ◽

Vol 59 (12) ◽

pp. 1215-1216

Author(s):

Huw M. L. Davies

Keyword(s):

New York ◽

Stereoselective Synthesis

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Stereoselective Synthesis of 2-Deoxy-β-glycosides From Glycal Precursors. 1. Stereochemistry of the Reactions of ?-Glucal Derivatives with Phenylsulfenyl Chloride and Phenylselenenyl Chloride

Tetrahedron ◽

10.1016/s0040-4020(97)00571-1 ◽

1997 ◽

Vol 53 (26) ◽

pp. 8825-8836

Author(s):

W Roush*

Keyword(s):

Stereoselective Synthesis

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