Abstract
The chemo- and stereoselective glycosidations of sulfinylglycosides and alcohols using a heteropoly acid, H3PW12O40, as a new promoter have been developed. (C) 2000 Elsevier Science Ltd.
Original language | English |
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Pages (from-to) | 10233-10237 |
Number of pages | 5 |
Journal | Tetrahedron Letters |
Volume | 41 |
Issue number | 52 |
DOIs | |
Publication status | Published - 2000 Dec 23 |
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Keywords
- α-mannopyranoside
- 2-deoxy-α-glucopyranoside
- Heteropoly acid
- Sulfinylglycoside
- Sulfoxide glycosidation
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
A novel promoter, heteropoly acid, mediated chemo- and stereoselective sulfoxide glycosidation reactions. / Nagai, Hideyuki; Matsumura, Shuichi; Toshima, Kazunobu.
In: Tetrahedron Letters, Vol. 41, No. 52, 23.12.2000, p. 10233-10237.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - A novel promoter, heteropoly acid, mediated chemo- and stereoselective sulfoxide glycosidation reactions
AU - Nagai, Hideyuki
AU - Matsumura, Shuichi
AU - Toshima, Kazunobu
PY - 2000/12/23
Y1 - 2000/12/23
N2 - The chemo- and stereoselective glycosidations of sulfinylglycosides and alcohols using a heteropoly acid, H3PW12O40, as a new promoter have been developed. (C) 2000 Elsevier Science Ltd.
AB - The chemo- and stereoselective glycosidations of sulfinylglycosides and alcohols using a heteropoly acid, H3PW12O40, as a new promoter have been developed. (C) 2000 Elsevier Science Ltd.
KW - α-mannopyranoside
KW - 2-deoxy-α-glucopyranoside
KW - Heteropoly acid
KW - Sulfinylglycoside
KW - Sulfoxide glycosidation
UR - http://www.scopus.com/inward/record.url?scp=0034707372&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034707372&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)01821-9
DO - 10.1016/S0040-4039(00)01821-9
M3 - Article
AN - SCOPUS:0034707372
VL - 41
SP - 10233
EP - 10237
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 52
ER -