Abstract
Palladium catalyzed decarboxylative allylation of active methylene compounds proceeded under mild neutral conditions using allylic carbonates, which are much more reactive than allylic acetates or phenoxides used commonly in the reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 4809-4812 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 23 |
| Issue number | 46 |
| DOIs | |
| Publication status | Published - 1982 |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates. / Tsuji, Jiro; Shimizu, Isao; Minami, Ichiro; Ohashi, Yukihiro.
In: Tetrahedron Letters, Vol. 23, No. 46, 1982, p. 4809-4812.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Facile Palladium catalyzed decarboxylative allylation of active methylene compounds under neutral conditions using allylic carbonates
AU - Tsuji, Jiro
AU - Shimizu, Isao
AU - Minami, Ichiro
AU - Ohashi, Yukihiro
PY - 1982
Y1 - 1982
N2 - Palladium catalyzed decarboxylative allylation of active methylene compounds proceeded under mild neutral conditions using allylic carbonates, which are much more reactive than allylic acetates or phenoxides used commonly in the reaction.
AB - Palladium catalyzed decarboxylative allylation of active methylene compounds proceeded under mild neutral conditions using allylic carbonates, which are much more reactive than allylic acetates or phenoxides used commonly in the reaction.
UR - http://www.scopus.com/inward/record.url?scp=0000423379&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0000423379&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)85719-6
DO - 10.1016/S0040-4039(00)85719-6
M3 - Article
VL - 23
SP - 4809
EP - 4812
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 46
ER -