N-PHENYLATION OF AMINO ACID DERIVATIVES

DOI: 10.1016/S0040-4039(00)95284-5

Source and publish data:

Tetrahedron Letters p. 937 - 940 (1989)

Update date:2022-08-03

Topics:

Authors:

Barton, Derek H. R.

Finet, Jean-Pierre

Khamsi, Jamal

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

Article abstract of DOI:10.1016/S0040-4039(00)95284-5

The selective mono N-phenylation of α-amino acid derivatives has been performed with triphenylbismuth diacetate in the presence of a catalytic amount of copper metal or copper diacylate.

Full text of DOI:10.1016/S0040-4039(00)95284-5

Products guided by the article

Product name:(S)-2-Phenylamino-pentanedioic acid dibenzyl ester

Cas No:123530-57-4

R&D Labs maybe for 123530-57-4

Ji'nan Orgachem Pharmaceutical Co.,Ltd

Contact:+86-531-82687810

Address:Jinan
Hybio Pharmaceutica Co.,Ltd

Contact:+86 755 26588093

Address:No.9 Linkong West Street, Hengdian Street, Huangpi District, Wuhan City, China.
WUHAN RISON TRADING CO.,LTD

Contact:0086-27-83607103/83642615

Address:No.498, Jianshe Ave, Wuhan, China
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China
Aminodiscovery Co.,Ltd.

Contact:+86-535-8888888

Address:No.161 Haishi Rd.

Relevant to this article

Pyrano[4, 3-d]pyrimidinium salts 3.* Reactions of 1, 3-dimethyl-2, 4-dioxo-1/7, 3/7-pyrano[4, 3-d]pyrimidinium salts with azomethines

Doi:10.1007/s11172-009-0196-y
(2009)
Polyfluorenylacetylene for near-infrared laser protection: Polymer synthesis, optical limiting mechanism and relationship between molecular structure and properties

Doi:10.1039/c7ra08499d
(2017)
A facile synthesis of 2,4-dialkoxy-, 2-alkoxy-4-phenoxy-, and 2,4-diphenoxy-6-trifluoromethyl-3,4-dihydro-2H-pyrans. Hetero-diels-alder reactions of trans-β-trifluoroacetylvinyl ethers with various vinyl ethers

Doi:10.1055/s-1989-27206
(1989)
Phosphorus-nitrogen compounds. 21. Syntheses, structural investigations, biological activities, and DNA interactions of new N/O spirocyclic phosphazene derivatives. the NMR behaviors of chiral phosphazenes with stereogenic centers upon the addition of chiral solvating agents

Doi:10.1021/ic100781v
(2010)
Synthesis of a spin-labeled anti-estrogen as a dynamic motion probe for the estrogen receptor ligand binding domain

Doi:10.1016/j.bmcl.2011.12.091
(2012)
An efficient microwave-assisted synthesis of 6,8-dihydroimidazo[1,2-a] [1,3,5] triazine derivatives

Doi:10.1002/jhet.378
(2010)

Article Doi