2005年3月
Suzuki-Miyaura cross-coupling of benzylic carbonates with arylboronic acids
ORGANIC LETTERS
- ,
- 巻
- 7
- 号
- 5
- 開始ページ
- 945
- 終了ページ
- 947
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1021/ol050078q
- 出版者・発行元
- AMER CHEMICAL SOC
The cross-coupling of benzylic carbonates with arylboronic acids gave the corresponding diarylmethanes in high yields by use of the palladium catalyst generated in situ from [Pd(eta(3)-C3H5)Cl](2) and 1,5-bis(diphenylphosphino)pentane (DPPPent). The Suzuki-Miyaura reaction using DPPPent-palladium catalyst is applicable to syntheses of a broad range of functionalized diarylmethanes.
- リンク情報
-
- DOI
- https://doi.org/10.1021/ol050078q
- CiNii Articles
- http://ci.nii.ac.jp/naid/80017208469
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/15727481
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000227313400050&DestApp=WOS_CPL
- ID情報
-
- DOI : 10.1021/ol050078q
- ISSN : 1523-7060
- CiNii Articles ID : 80017208469
- PubMed ID : 15727481
- Web of Science ID : WOS:000227313400050