Details
| Original language | English |
|---|---|
| Pages (from-to) | 2236-2238 |
| Number of pages | 3 |
| Journal | SYNLETT |
| Issue number | 14 |
| Publication status | Published - 2 Sept 2005 |
Abstract
The synthesis of the C19-C26 methyl ketone of amphidinolide H2 is described employing a stereoselective catalytic vinylogous Mukaiyama aldol reaction. Selective dihydroxylation and deoxygenation completes the synthesis of the C19-C26 segment.
Keywords
- Aldol reactions, Deoxygenation, Dihydroxylation, Natural products, Vinylogous
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
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In: SYNLETT, No. 14, 02.09.2005, p. 2236-2238.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Synthesis of the C19-C26 segment of amphidinolide H2
AU - Liesener, Florian P.
AU - Kalesse, Markus
PY - 2005/9/2
Y1 - 2005/9/2
N2 - The synthesis of the C19-C26 methyl ketone of amphidinolide H2 is described employing a stereoselective catalytic vinylogous Mukaiyama aldol reaction. Selective dihydroxylation and deoxygenation completes the synthesis of the C19-C26 segment.
AB - The synthesis of the C19-C26 methyl ketone of amphidinolide H2 is described employing a stereoselective catalytic vinylogous Mukaiyama aldol reaction. Selective dihydroxylation and deoxygenation completes the synthesis of the C19-C26 segment.
KW - Aldol reactions
KW - Deoxygenation
KW - Dihydroxylation
KW - Natural products
KW - Vinylogous
UR - http://www.scopus.com/inward/record.url?scp=24744471404&partnerID=8YFLogxK
U2 - 10.1055/s-2005-872236
DO - 10.1055/s-2005-872236
M3 - Article
AN - SCOPUS:24744471404
SP - 2236
EP - 2238
JO - SYNLETT
JF - SYNLETT
SN - 0936-5214
IS - 14
ER -