Abstract
(Chemical Equation Presented) Chemical synthesis of a bacterial glycolipid BbL1 is reported in two steps starting from per-0-TMS D-galactose. The key features are glycosyl iodide mediated β-stereoselective glycosylation in the absence of neighboring group participation and regioseiective acylation.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4739-4742 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 10 |
| Issue number | 21 |
| DOIs | |
| State | Published - Dec 1 2008 |
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ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
Cite this
Two-step synthesis of the immunogenic bacterial glycolipid BbGL1. / Kulkarni, Suvarn S.; Gervay-Hague, Jacquelyn.
In: Organic Letters, Vol. 10, No. 21, 01.12.2008, p. 4739-4742.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Two-step synthesis of the immunogenic bacterial glycolipid BbGL1
AU - Kulkarni, Suvarn S.
AU - Gervay-Hague, Jacquelyn
PY - 2008/12/1
Y1 - 2008/12/1
N2 - (Chemical Equation Presented) Chemical synthesis of a bacterial glycolipid BbL1 is reported in two steps starting from per-0-TMS D-galactose. The key features are glycosyl iodide mediated β-stereoselective glycosylation in the absence of neighboring group participation and regioseiective acylation.
AB - (Chemical Equation Presented) Chemical synthesis of a bacterial glycolipid BbL1 is reported in two steps starting from per-0-TMS D-galactose. The key features are glycosyl iodide mediated β-stereoselective glycosylation in the absence of neighboring group participation and regioseiective acylation.
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UR - http://www.scopus.com/inward/citedby.url?scp=58149156305&partnerID=8YFLogxK
U2 - 10.1021/ol801780c
DO - 10.1021/ol801780c
M3 - Article
C2 - 18798644
AN - SCOPUS:58149156305
VL - 10
SP - 4739
EP - 4742
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 21
ER -