SYNTHESIS OF BENZO-1,4-DIOXANE IN THE PRESENCE OF INTERPHASE CATALYSTS

DOI: 10.1007/BF00516441

Source and publish data:

Chemistry of Heterocyclic Compounds p. 832 - 833 (1983)

Update date:2022-08-16

Topics:

Authors:

Lyushin, M.M.

Bakus, Yalda Pimanos

Budzema, Khamada

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

Article abstract of DOI:10.1007/BF00516441

Quaternary ammonium salts markedly accelerate the formation of benzo-1,4-dioxane from 1,2-dibromoethane and pyrocatechol under the influence of aqueous alkali and increase its yield.

Full text of DOI:10.1007/BF00516441

Products guided by the article

Product name:1,4-Benzodioxan

Cas No:493-09-4

R&D Labs maybe for 493-09-4

Anhui Gusheng Import&Export CO.,LTD

Contact:86-551-63662296

Address:Jinzhai Road NO.162 ,hefei, china
Shanghai KFSL Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-39971718

Address:859 jiadingchengliu shanghai
Anhui Dexinjia Biopharm Co., Ltd

Contact:+86-531-82375818

Address:9 Hexie Road, kaifaqu, Taihe
Shantou Baokang Pharmaceutical Co., Ltd.

Contact:+86-754-88873487

Address:5/F B Block Huangshan Bldg Huangshan Rd Shantou
CHEM PLUS

Contact:0027-717-456976

Address:2ND FLOOR, 325 VAUSE ROAD, OVERPORT, 4001, SOUTH AFRICA

Relevant to this article

Synthesis, Docking, and Bioavailability of 2′-Oxo-3-phenylspiro[cyclopropane-1,3′-indoline]-2,2-dicarbonitriles as Antibacterial Agents In Silico

Doi:10.1002/jhet.3396
(2019)
Palladium supported on metal–organic framework as a catalyst for the hydrogenation of nitroarenes under mild conditions

Doi:10.1002/aoc.5607
(2020)
Selective hydrogenolysis of glycerol to 1,3-propanediol over a Pt/WO ₃/TiO₂/SiO₂ catalyst in aqueous media

Doi:10.1016/j.apcata.2010.10.002
(2010)
Reactive sulfur species: Kinetics and mechanisms of the oxidation of cysteine by hypohalous acid to give cysteine sulfenic acid

Doi:10.1021/ja0737218
(2007)
Doi:10.1007/BF00921482
()
Synthesis and characterization of poly(tetramethylsilarylenesiloxane) derivatives with oligothiophene based moiety

Doi:10.1016/j.polymer.2019.01.069
(2019)

Article Doi