抄録
The nucleophilic substitution of diarylmethyl carbonates with malonate carbanions proceeded in the presence of [Pd(π-C3H 5)(cod)]BF4-Cy-Xantphos, giving the desired (diarylmethyl)malonates in up to 90% yield. The yield was extremely affected by choice of the phosphine ligand.
| 元の言語 | 英語 |
|---|---|
| ページ（範囲） | 528-529 |
| ページ数 | 2 |
| ジャーナル | Chemistry Letters |
| 巻 | 36 |
| 発行部数 | 4 |
| DOI | |
| 出版物ステータス | 出版済み - 4 5 2007 |
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All Science Journal Classification (ASJC) codes
- Chemistry(all)
これを引用
Palladium-catalyzed nucleophilic substitution of diarylmethyl carbonates with malonate carbanions. / Kuwano, Ryoichi; Kusano, Hiroki.
：: Chemistry Letters, 巻 36, 番号 4, 05.04.2007, p. 528-529.研究成果: ジャーナルへの寄稿 › 記事
}
TY - JOUR
T1 - Palladium-catalyzed nucleophilic substitution of diarylmethyl carbonates with malonate carbanions
AU - Kuwano, Ryoichi
AU - Kusano, Hiroki
PY - 2007/4/5
Y1 - 2007/4/5
N2 - The nucleophilic substitution of diarylmethyl carbonates with malonate carbanions proceeded in the presence of [Pd(π-C3H 5)(cod)]BF4-Cy-Xantphos, giving the desired (diarylmethyl)malonates in up to 90% yield. The yield was extremely affected by choice of the phosphine ligand.
AB - The nucleophilic substitution of diarylmethyl carbonates with malonate carbanions proceeded in the presence of [Pd(π-C3H 5)(cod)]BF4-Cy-Xantphos, giving the desired (diarylmethyl)malonates in up to 90% yield. The yield was extremely affected by choice of the phosphine ligand.
UR - http://www.scopus.com/inward/record.url?scp=34248538139&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34248538139&partnerID=8YFLogxK
U2 - 10.1246/cl.2007.528
DO - 10.1246/cl.2007.528
M3 - Article
AN - SCOPUS:34248538139
VL - 36
SP - 528
EP - 529
JO - Chemistry Letters
JF - Chemistry Letters
SN - 0366-7022
IS - 4
ER -