Details
| Original language | English |
|---|---|
| Pages (from-to) | 696-699 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 14 |
| Issue number | 3 |
| Publication status | Published - 19 Jan 2012 |
Abstract
A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-forming radical Ueno - Stork cyclization to form the heterocyclic core.
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Chemistry(all)
- Physical and Theoretical Chemistry
- Chemistry(all)
- Organic Chemistry
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In: Organic Letters, Vol. 14, No. 3, 19.01.2012, p. 696-699.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - A total synthesis of millingtonine a
AU - Wegner, Jens
AU - Ley, Steven V.
AU - Kirschning, Andreas
AU - Hansen, Anne Lene
AU - Montenegro Garcia, Javier
AU - Baxendale, Ian R.
PY - 2012/1/19
Y1 - 2012/1/19
N2 - A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-forming radical Ueno - Stork cyclization to form the heterocyclic core.
AB - A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-forming radical Ueno - Stork cyclization to form the heterocyclic core.
UR - http://www.scopus.com/inward/record.url?scp=84856753223&partnerID=8YFLogxK
U2 - 10.1021/ol203158p
DO - 10.1021/ol203158p
M3 - Article
C2 - 22260734
AN - SCOPUS:84856753223
VL - 14
SP - 696
EP - 699
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 3
ER -