Details
| Original language | English |
|---|---|
| Article number | ST-2013-B0302-L |
| Pages (from-to) | 1105-1108 |
| Number of pages | 4 |
| Journal | SYNLETT |
| Volume | 24 |
| Issue number | 9 |
| Publication status | Published - 2013 |
Abstract
The vinylogous Mukaiyama aldol reaction (VMAR) allows the rapid assembly of polyketide building blocks in complex natural product syntheses. Here we describe how different diastereomers can be obtained efficiently from commercially available Roche ester.
Keywords
- Mukaiyama, polyketides, Roche ester, substrate control, vinylogous aldol
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
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In: SYNLETT, Vol. 24, No. 9, ST-2013-B0302-L, 2013, p. 1105-1108.
Research output: Contribution to journal › Review article › Research › peer review
}
TY - JOUR
T1 - Diastereodivergent vinylogous Mukaiyama aldol reaction
AU - Landsberg, Dirk
AU - Hartmann, Olaf
AU - Eggert, Ulrike
AU - Kalesse, Markus
PY - 2013
Y1 - 2013
N2 - The vinylogous Mukaiyama aldol reaction (VMAR) allows the rapid assembly of polyketide building blocks in complex natural product syntheses. Here we describe how different diastereomers can be obtained efficiently from commercially available Roche ester.
AB - The vinylogous Mukaiyama aldol reaction (VMAR) allows the rapid assembly of polyketide building blocks in complex natural product syntheses. Here we describe how different diastereomers can be obtained efficiently from commercially available Roche ester.
KW - Mukaiyama
KW - polyketides
KW - Roche ester
KW - substrate control
KW - vinylogous aldol
UR - http://www.scopus.com/inward/record.url?scp=84876713749&partnerID=8YFLogxK
U2 - 10.1055/s-0033-1338933
DO - 10.1055/s-0033-1338933
M3 - Review article
AN - SCOPUS:84876713749
VL - 24
SP - 1105
EP - 1108
JO - SYNLETT
JF - SYNLETT
SN - 0936-5214
IS - 9
M1 - ST-2013-B0302-L
ER -