Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4

DOI: 10.1016/S0040-4039(00)73351-X

Source and publish data:

Tetrahedron Letters p. 4349 - 4350 (1994)

Update date:2022-08-11

Topics:

Authors:

Beugelmans, Rene

Bourdet, Sebastien

Bigot, Antony

Zhu, Jieping

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(00)73351-X

Treatment of aryl allyl ethers with catalytic amounts of Pd(PPh₃)₄ and NaBH₄ at room temperature afforded the parent phenol in high yield under non-hydrolytic conditions.

Full text of DOI:10.1016/S0040-4039(00)73351-X

Products guided by the article

Product name:4-Nitrophenol

Cas No:100-02-7

Relevant to this article

A novel fluorescent long-chain fatty acid-substituted dye: labeling and biodegrading of Microthrix parvicella

Doi:10.1039/C8RA06986G
(2018)
Asymmetric Catalytic Syntheses of Pharmaceutically Important β-Amino-α-Hydroxyl Esters by Enantioselective Aminolysis of Methyl Phenylglycidate

Doi:10.1002/cctc.201601208
(2017)
Doi:10.1007/BF00907388
(1974)
The mechanism of the formation and hydrolysis of phenyl ether in the basic hydrolysis of chlorobenzene.

Doi:10.1021/ja01008a033
(1968)
Persistent, well-defined, monodisperse, π-conjugated organic nanoparticles via G-quadruplex self-assembly

Doi:10.1021/ja908537k
(2010)
Photocatalytic hydrogenation coupling of acetone into pinacol using formic acid as hydrogen source

Doi:10.1246/cl.170781
(2017)

Article Doi

Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4

DOI: 10.1016/S0040-4039(00)73351-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)73351-X

Full text of DOI:10.1016/S0040-4039(00)73351-X

Products guided by the article

Relevant to this article

Hot Product