Reactions of Lithium Aluminium Hydride in Hydrocarbon Solvents. Selective Demethylation of Some Substituted Methyl Phenyl Ethers

DOI: 10.1039/c39800000507

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 507 - 508 (1980)

Update date:2022-08-29

Topics:

Authors:

Carrol, John F.

Kulkowit, Sunanta

McKervey, M. Anthony

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

Article abstract of DOI:10.1039/c39800000507

Lithium aluminium hydride in benzene or heptane is an effective reagent for selective demthylation of methyl phenyl ethers having additional ether functions in the immediate vicinity of the reaction site.

Full text of DOI:10.1039/c39800000507

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:Pyrocatechol

Cas No:120-80-9

R&D Labs maybe for 120-80-9

Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK
Hangzhou Gangjin Chemical Co.,Ltd.(expird)

Contact:+86-571-85109780

Address:707 Zhejiang Minhang Bldg., No.290 Zhongshan North Road, Hangzhou 310003, China
Shandong Hongxiang Zinc Co., Ltd

Contact:086-0311-66187879

Address:DaWang developing zone
Jinan Decheng Hemu Medical Technology Co.，Ltd.

Contact:+86-531-68650525

Address:NO.554 Zhengfeng Road High-new Technology Development Zone
Xi'an Tizan Tech & Industry Co., Ltd.

Contact:86-18629066522

Address:C3009 TANG FENG INTERNATIONAL PLAZA, NO.18 FENGHUI NAN ROAD, XI'AN HIGH TECH ZONE, 710075 CHINA.

Relevant to this article

Anion–π Interactions in Light-Induced Reactions: Role in the Amidation of (Hetero)aromatic Systems with Activated N-Aryloxyamides

Doi:10.1002/chem.201903055
(2019)
Quantification of N-acetylcysteamine activated methylmalonate incorporation into polyketide biosynthesis

Doi:10.3762/bjoc.9.75
(2013)
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry

Doi:10.1016/j.bmc.2019.01.031
(2019)
A copper-catalyzed approach for the synthesis of asymmetrical disubstituted 1,2,4-thiadiazoles via elemental sulfur-mediated decarboxylative redox cyclization

Doi:10.1016/j.tetlet.2020.152744
(2021)
Docking investigation and binding interaction of benzimidazole derivative with bovine serum albumin

Doi:10.1016/j.jphotobiol.2012.08.018
(2012)
Doi:10.1021/ja01259a503
(1942)

Article Doi