Abstract
Chiral trans-enals derived from 2-deoxypyranoses by ylide-induced β-elimination were exploited for the synthesis and stereochemical revision of a novel, marine eicosanoid.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2971-2974 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 31 |
| Issue number | 21 |
| DOIs | |
| State | Published - 1990 |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Synthesis and stereochemical revision of a bioactive dihydroxyeicosanoid isolated from the red marine alga farlowia mollis. / Lumin, Sun; Falck, J R.
In: Tetrahedron Letters, Vol. 31, No. 21, 1990, p. 2971-2974.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthesis and stereochemical revision of a bioactive dihydroxyeicosanoid isolated from the red marine alga farlowia mollis
AU - Lumin, Sun
AU - Falck, J R
PY - 1990
Y1 - 1990
N2 - Chiral trans-enals derived from 2-deoxypyranoses by ylide-induced β-elimination were exploited for the synthesis and stereochemical revision of a novel, marine eicosanoid.
AB - Chiral trans-enals derived from 2-deoxypyranoses by ylide-induced β-elimination were exploited for the synthesis and stereochemical revision of a novel, marine eicosanoid.
UR - http://www.scopus.com/inward/record.url?scp=0025347733&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025347733&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)89001-2
DO - 10.1016/S0040-4039(00)89001-2
M3 - Article
AN - SCOPUS:0025347733
VL - 31
SP - 2971
EP - 2974
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 21
ER -