Details
| Original language | English |
|---|---|
| Pages (from-to) | 1264-1268 |
| Number of pages | 5 |
| Journal | Synlett |
| Issue number | 8 |
| Publication status | Published - 18 Apr 2007 |
Abstract
The enantioselective synthesis of two new proansamitocin derivatives is described. Macrocyclization is achieved by ring-closing metathesis of appropriate alkene and diene precursors.
Keywords
- Ansamitocins, Macrolactam antibiotics, Natural product synthesis, Ring-closing metathesis
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
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In: Synlett, No. 8, 18.04.2007, p. 1264-1268.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Total syntheses of new proansamitocin derivatives by ring-closing metathesis
AU - Meyer, Axel
AU - Kirschning, Andreas
PY - 2007/4/18
Y1 - 2007/4/18
N2 - The enantioselective synthesis of two new proansamitocin derivatives is described. Macrocyclization is achieved by ring-closing metathesis of appropriate alkene and diene precursors.
AB - The enantioselective synthesis of two new proansamitocin derivatives is described. Macrocyclization is achieved by ring-closing metathesis of appropriate alkene and diene precursors.
KW - Ansamitocins
KW - Macrolactam antibiotics
KW - Natural product synthesis
KW - Ring-closing metathesis
UR - http://www.scopus.com/inward/record.url?scp=34249795484&partnerID=8YFLogxK
U2 - 10.1055/s-2007-977441
DO - 10.1055/s-2007-977441
M3 - Article
AN - SCOPUS:34249795484
SP - 1264
EP - 1268
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 8
ER -