Synthese von α-Trifluormethyl-substituierten Asparaginsaeuren und Ihren Derivaten

DOI: 10.1016/S0022-1139(00)81044-1

Source and publish data:

Journal of Fluorine Chemistry p. 429 - 434 (1988)

Update date:2022-08-03

Topics:

Authors:

Burger, Klaus

Gaa, Karl

Geith, Klaus

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

Article abstract of DOI:10.1016/S0022-1139(00)81044-1

Syntheses of α-trifluoromethyl aspartic acid, β-substituted, and β,β-disubstituted α-trifluoromethyl aspartic acids are described.

Full text of DOI:10.1016/S0022-1139(00)81044-1

Products guided by the article

Product name:5(4H)-Oxazolone, 2-phenyl-4-(2-propenyl)-4-(trifluoromethyl)-

Cas No:114490-65-2

R&D Labs maybe for 114490-65-2

Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.
Suzhou Jingye Medicine & Chemical Co., Ltd

Contact:+86-512-66658588

Address:No. 88, Sanlian Street, Jinfeng Road, Suzhou New District, Jiangsu Province, P. R. China
Shanghai Korey Pharm Co.,Ltd.(expird)

Contact:021-61840961 021-61840962

Address:No.157,Zhuguang Rd, Qingpu, Shanghai, China
Yueyang Hudex Pharmaceuticals Ltd.

Contact:0730-8748800

Address:Wujiang Bridge，Yueyang Economy & Technology Development Zone
Hotechem Shanghai Co., Ltd

Contact:13120882795；+86-21-34621078;+86-021-31122318

Address:Suite 2,No.2715 Longwu Road

Relevant to this article

Redox-Neutral Photocatalytic Cyclopropanation via Radical/Polar Crossover

Doi:10.1021/jacs.8b05243
(2018)
Cyclopropanation/Carboboration Reactions of Enynes with B(C₆F₅)₃

Doi:10.1021/jacs.5b09311
(2015)
An efficacious protocol for the oxidation of 3,4-dihydropyrimidin-2(1H)- ones using pyridinium chlorochromate as catalyst

Doi:10.1071/CH07432
(2008)
Effects of 5-O-Ribosylation of Aminoglycosides on Antimicrobial Activity and Selective Perturbation of Bacterial Translation

Doi:10.1021/acs.jmedchem.6b00793
(2016)
Selective C-H activation of haloalkanes using a rhodiumtrispyrazolylborate complex

Doi:10.1021/ja9002316
(2009)
Synthesis, biological evaluation, and molecular docking of Ugi products containing a zinc-chelating moiety as novel inhibitors of histone deacetylases

Doi:10.1021/jm801529c
(2009)

Article Doi