Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4
Beugelmans, Rene; Bourdet, Sebastien; Bigot, Antony; Zhu, Jieping
1994

Abstract

Treatment of aryl allyl ethers with catalytic amts. of Pd(PPh3)4 and NaBH4 at room temp. afforded the parent phenol in high yield under non-hydrolytic conditions. E.g., treatment of ether I (R = allyl) with NaBH4 in the presence of Pd(PPh3)4 in THF gave 97% I (R = H). [on SciFinder (R)]

Details

Title Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4
Author(s) Beugelmans, Rene ; Bourdet, Sebastien ; Bigot, Antony ; Zhu, Jieping
Published in Tetrahedron Letters
Volume 35
Issue 25
Pages 4349-50
Date 1994
ISSN 0040-4039
Keywords
Note CAN 121:107593
21-2
General Organic Chemistry
Institut de Chimie des Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.
Journal
written in English.
127132-38-1P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and reductive deprotection of, with sodium borohydride in presence of tetrakis(triphenylphosphine)palladium catalyst); 98-54-4P; 100-02-7P; 621-37-4P; 3978-80-1P; 156945-64-1P; 156945-65-2P; 156945-66-3P; 156945-67-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of); 1568-66-7; 24806-16-4; 156945-58-3; 156945-59-4; 156945-60-7; 156945-61-8; 156945-62-9; 156945-63-0 Role: PROC (Process) (reductive deprotection of, with sodium borohydride in presence of tetrakis(triphenylphosphine)palladium catalyst)
DOI https://doi.org/10.1016/S0040-4039(00)73351-X
Laboratories LSPN
Record Appears in Scientific production and competences > SB - School of Basic Sciences > ISIC - Institute of Chemical Sciences and Engineering > LSPN - Laboratory of synthesis and natural products
Peer-reviewed publications
Work outside EPFL
Journal Articles
Published
Record creation date 2010-11-25

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