HALOGENATION OF FLUOROALKYL-SUBSTITUTED β-KETOESTERS

DOI: 10.1007/BF01141716

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1016 - 1022 (1984)

Update date:2022-08-04

Topics:

Authors:

Saloutin, V. I.

Skryabina, Z. E.

Rudaya, M. N.

Pashkevich, K. I.

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

Article abstract of DOI:10.1007/BF01141716

Full text of DOI:10.1007/BF01141716

Products guided by the article

Product name:Butanoic acid, 2,2-dibromo-4,4,4-trifluoro-3-oxo-, methyl ester

Cas No:93032-04-3

R&D Labs maybe for 93032-04-3

Simagchem Corporation

website:http://www.simagchem.com

Contact:+86-592-2680277

Address:21/F Hualong Office Building,No.6 Hubin East Road, Xiamen,China
Anhui Xinyuan Technology Co.,Ltd

website:http://www.ahxytech.com/

Contact:0086-559-3515800

Address:Huangshan City of Anhui Province Huizhou Huizhou District Road, 21-9
NINGBO YINZHOU PRECISE COLOR CO.,LTD.

Contact:86-574-88139809 86-574-83033159

Address:Qiming Road,Yinzhou,Ningbo,China
Tai zhou world Pharm & Chem Co., Ltd

Contact:+86-576-85301198

Address:Rome 1001,wangjiang plaza,unti 2,jinshan east Road linhai,zhejiang,china
Tangshan Moneide Trading Co., Ltd.

Contact:+86-315-8309571

Address:2-7-420 Jidong Building Materials Commercial Center, Tangshan, Hebei, 064000 China

Relevant to this article

Doi:10.1021/jo01070a021
(1961)
Kinetics and Mechanism of Hydrolysis of 4-Phenylallophanates

Doi:10.1039/P29840001233
(1984)
The Ability of an α-Aminoisobutyric Acid Residue to Promote Helical Folding in Oligopeptides

Doi:10.1246/bcsj.58.1731
(1985)
A competitive and highly selective 7-, 6- And 5-annulation with 1,3-migration through C-H and N-H-alkyne coupling

Doi:10.1039/c9cc07360d
(2020)
Structural characterisation of a series of acetylide-functionalised oligopyridines and the synthesis, characterisation and optical spectroscopy of platinum di-ynes and poly-ynes containing oligopyridyl linker groups in the backbone

Doi:10.1039/b110658a
(2002)
Design and synthesis of 4-anilinoquinazolines as Raf kinase inhibitors. Part 1. Selective B-Raf/B-Raf^V600E and potent EGFR/VEGFR2 inhibitory 4-(3-hydroxyanilino)-6-(1H-1,2,3-triazol-4-yl)quinazolines

Doi:10.1016/j.bioorg.2021.104715
(2021)

Article Doi