Abstract
Trialkylaluminium-mediated alkylation of enol phosphates under the CO bond cleavage is performed stereospecifically in the presence of a catalytic amount of Pd(PPh3)4. Alkenylation and alkynylation are also described.
| Original language | English |
|---|---|
| Pages (from-to) | 2531-2534 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 21 |
| Issue number | 26 |
| DOIs | |
| Publication status | Published - 1980 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Carboncarbon bond formation by cross-coupling of enol phosphates with organoaluminium compounds catalyzed by palladium(O) complex. / Takai, Kazuhiko; Oshima, Koichiro; Nozaki, Hitosi.
In: Tetrahedron Letters, Vol. 21, No. 26, 1980, p. 2531-2534.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Carboncarbon bond formation by cross-coupling of enol phosphates with organoaluminium compounds catalyzed by palladium(O) complex
AU - Takai, Kazuhiko
AU - Oshima, Koichiro
AU - Nozaki, Hitosi
PY - 1980
Y1 - 1980
N2 - Trialkylaluminium-mediated alkylation of enol phosphates under the CO bond cleavage is performed stereospecifically in the presence of a catalytic amount of Pd(PPh3)4. Alkenylation and alkynylation are also described.
AB - Trialkylaluminium-mediated alkylation of enol phosphates under the CO bond cleavage is performed stereospecifically in the presence of a catalytic amount of Pd(PPh3)4. Alkenylation and alkynylation are also described.
UR - http://www.scopus.com/inward/record.url?scp=0012152398&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0012152398&partnerID=8YFLogxK
U2 - 10.1016/0040-4039(80)80120-1
DO - 10.1016/0040-4039(80)80120-1
M3 - Article
AN - SCOPUS:0012152398
VL - 21
SP - 2531
EP - 2534
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 26
ER -