Reactions of Halogenated o-Quinol Acetates with Isopropylmagnesium Bromide and Di-isopropylmagnesium. Mechanism for Formation of Ethers, Reduction Products, and m-Isopropylphenols

DOI: 10.1039/c39840001617

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1617 - 1619 (1984)

Update date:2022-08-05

Topics:

Authors:

Miller, Bernard

Haggerty, John G.

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

Article abstract of DOI:10.1039/c39840001617

A mechanism is proposed to account for the nature and the variations in yields of products from reactions of Grignard reagents with halogenated o-quinol acetates.

Full text of DOI:10.1039/c39840001617

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

View Article Online

Products guided by the article

Product name:Phenol, 2-bromo-4,6-dimethyl-3-(1-methylethyl)-

Cas No:95717-60-5

R&D Labs maybe for 95717-60-5

Beijing Top Science biological technology co., LTD

Contact:+86-13439059536

Address:15-1705 jre three mile, Beijing 100000,CHINA
Nanjing HuiBaiShi Biotechnology Co.,Ltd.

Contact:+86 (25)58745219

Address:No.606 Ningliu Road,LiuHe District.
Xi'an Unique Electronic and Chemical Co., Ltd.

Contact:+86-029-88238008

Address:1703# B BUILDING WEST ELECTRONIC ZONE, XI'AN, CHINA
NanJing KaiHeng Chemical CO., LTD.

Contact:+86-25-85768391

Address:RM.1704, D, WANDA PLAZA, NO.110, MIDDLE JIANGDONG ROAD, NANJING, CHINA
Shanghai Run-Biotech Co., Ltd.

website:http://www.run-biotech.com

Contact:+86-21-31576854/57171705 / 57171706

Address:second floor, building 3, No.999, jiangyue Road, minghang District, Shanghai, China

Relevant to this article

Doi:10.1007/BF00942917
()
Doi:10.1021/jo01121a011
(1955)
Cardiotonic agents. 4. Synthesis and biological evaluation of N-substituted 2,4,4a,5-tetrahydro-3H-indeno[1,2-c]pyridazin-3-ones: Rigid structures derived from CI-930 and analogues

Doi:10.1021/jm00161a003
(1986)
Quantitative study of photochromic transformations of diarylethene derivatives with either perhydrocyclopentene or oxazolone or lactone units

Doi:10.1016/j.dyepig.2014.02.013
(2014)
Thermal Ring Annulation of α-Vinylcinnamate Methyl Esters. A Method for the Generation of 3,4-Dihydro-2-naphthoate and 2-Naphthoate Methyl Esters

Doi:10.1021/jo00255a010
(1988)
Synthetic Application of Tris(methylthio)methyl Salts. An Efficient Route to Trithioorthocarboxylic Esters from Strongly Activated Aromatic and Heteroaromatic Systems

Doi:10.1055/s-1988-27455
(1988)

Article Doi