Scholarly article on Phenol,2,2',2''-methylidynetris[4-methyl- 7573-17-3 from Journal of the Chemical Society C: Organic p. 1519 - 1521

DOI: 10.1039/j39660001519

Source and publish data:

Journal of the Chemical Society C: Organic p. 1519 - 1521 (1966)

Update date:2022-08-03

Topics:

Authors:

Chan,S.C.

Driver,J.E.

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

Article abstract of DOI:10.1039/j39660001519

Full text of DOI:10.1039/j39660001519

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

View Article Online

Products guided by the article

Product name:Phenol,2,2',2''-methylidynetris[4-methyl-

Cas No:7573-17-3

R&D Labs maybe for 7573-17-3

HENAN NEW BLUE CHEMICAL CO.,LTD

website:http://www.newbluechem.com

Contact:86-371-55170693/55170694

Address:Zhengzhou International Trade New Territory,Jinshui District,Zhengzhou ,China
shijiazhuang alkay chemicals co..ltd(expird)

Contact:86-311-67692035

Address:2601,juntang building,qiaodong district,shijiazhuang
SHIFANG SUHONG CHEMICAL CO.,LTD

Contact:+86-838-2224563

Address:Room 1207 Zongchen Sunshine No.128 Taishan South Road,Deyang City,Sichuan China
Jiangsu Dacheng Pharmaceutical and Chemical Co.,Ltd

Contact:+86-0517-87036900

Address:Chuzhou Chemical park, Huai'an, Jiangsu Province
Synasia Inc

Contact:17316303296

Address:240 Amboy Ave

Relevant to this article

Copper-catalysed: Ortho -selective C-H bond functionalization of phenols and naphthols with α-aryl-α-diazoesters

Doi:10.1039/d0cc04495d
(2020)
Hydroboration of vinylglycine and allylglycine as a route to boron- derivatives of α-amino acids

Doi:10.1016/0040-4039(96)01062-3
(1996)
Hydroboration Reaction and Mechanism of Carboxylic Acids using NaNH₂(BH₃)₂, a Hydroboration Reagent with Reducing Capability between NaBH₄and LiAlH₄

Doi:10.1021/acs.joc.1c00302
(2021)
MARASMIC ACID-I. TOTAL SYNTHESIS OF (+/-)-ISOMARASMIC ACID

Doi:10.1016/0040-4020(80)80186-4
(1980)
3-Hydroxy-3-methylglutaryl-coenzyme A Reductase Inhibitors. 4. Side Chain Ester Derivatives of Mevinolin

Doi:10.1021/jm00155a040
(1986)
Doi:10.1021/jo01122a009
(1955)

Article Doi

DOI: 10.1039/j39660001519