PENTAFLUOROPEROXYBENZOIC ACID - A NEW HIGHLY ACTIVE AND STABLE OXIDIZING REAGENT

DOI: 10.1007/BF00950292

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 1051 - 1054 (1981)

Update date:2022-08-04

Topics:

Authors:

Dzhemilev, U. M.

Vostrikov, N. S.

Moiseenkov, A. M.

Tolstikov, G. A.

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

Article abstract of DOI:10.1007/BF00950292

Full text of DOI:10.1007/BF00950292

Products guided by the article

Product name:2,3,4,5,6-pentafluoroperoxybenzoic acid

Cas No:71208-93-0

R&D Labs maybe for 71208-93-0

Shanghai Kangxin Chemical Co., Ltd

Contact:+86 21 60717227

Address:118,Ganbai Village,Waigang Town,Jiading District,Shanghai
Sinonine Industry Co.,Ltd

Contact:86+21-56421993

Address:3F,BUILDING 10,NO.2889 JINKE ROAD, SHANGHAI.
Qingdao BZ Oligo Biotech Co., Ltd

Contact:86-532-8192627

Address:Room 806, D&D Fortune Center, No. 182-6 Haier Road, Qingdao 266061, China
Improve Medical Technology(Nanxiong) Co., Ltd

Contact:86-751-3836997

Address:No.33, Pingan First Road, Fine Chemical Industry Base, Nanxiong City, Shaoguan, Guangdong, China
Henan Techway Chemical Co.,Ltd.

website:http://www.techwaychem.com

Contact:+86-371-66380080

Address:No.27 Shunhe Road,

Relevant to this article

Palladium-Catalyzed Decarboxylation-Allylation of Allylic Esters of α-Substituted β-Keto Carboxylic, Malonic, Cyanoacetic, and Nitroacetic Acids

Doi:10.1021/jo00390a007
(1987)
Doi:10.1246/cl.1979.409
(1979)
Tandem hetero Diels-Alder reaction: Synthesis of oxygenated macrocycles

Doi:10.1021/ol007040s
(2001)
Structure-based design of ester compounds to inhibit MLL complex catalytic activity by targeting mixed lineage leukemia 1 (MLL1)–WDR5 interaction

Doi:10.1016/j.bmc.2016.09.073
(2016)
Structural dynamics and ligand mobility in carboxylate and dithiocarbamate complexes of Ru(II) containing 1,1′-bis (diphenylphosphino)ferrocene (dppf)

Doi:10.1016/j.jorganchem.2003.08.037
(2003)
Organic base-catalysed solvent-tuned chemoselective carbotrifluoromethylation and oxytrifluoromethylation of unactivated alkenes

Doi:10.1039/c6cc00364h
(2016)

Article Doi