Details
| Original language | English |
|---|---|
| Pages (from-to) | 655-657 |
| Number of pages | 3 |
| Journal | SYNLETT |
| Issue number | 4 |
| Publication status | Published - 4 Mar 2005 |
Abstract
The synthesis of the C13-C23 segment of tedanolide is described making use of orthogonal protecting groups in the construction of the carbon skeleton and for the selective liberation of hydroxyl groups in the endgame of the total synthesis.
Keywords
- Aldol, Natural product, Protecting groups, Tedanolide
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
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In: SYNLETT, No. 4, 04.03.2005, p. 655-657.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Synthesis of the C13-C23 segment of tedanolide
AU - Ehrlich, Gunnar
AU - Kalesse, Markus
PY - 2005/3/4
Y1 - 2005/3/4
N2 - The synthesis of the C13-C23 segment of tedanolide is described making use of orthogonal protecting groups in the construction of the carbon skeleton and for the selective liberation of hydroxyl groups in the endgame of the total synthesis.
AB - The synthesis of the C13-C23 segment of tedanolide is described making use of orthogonal protecting groups in the construction of the carbon skeleton and for the selective liberation of hydroxyl groups in the endgame of the total synthesis.
KW - Aldol
KW - Natural product
KW - Protecting groups
KW - Tedanolide
UR - http://www.scopus.com/inward/record.url?scp=15444372188&partnerID=8YFLogxK
U2 - 10.1055/s-2005-862391
DO - 10.1055/s-2005-862391
M3 - Article
AN - SCOPUS:15444372188
SP - 655
EP - 657
JO - SYNLETT
JF - SYNLETT
SN - 0936-5214
IS - 4
ER -