Scholarly article on 2-methyl-4-benzyloxy-1-naphthol 53772-21-7 from Journal of the American Chemical Society p. 8046 - 8054

DOI: 10.1021/ja00833a035

Source and publish data:

Journal of the American Chemical Society p. 8046 - 8054 (1974)

Update date:2022-08-04

Topics:

Authors:

Snyder,C.D.

Rapoport,H.

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

Article abstract of DOI:10.1021/ja00833a035

Full text of DOI:10.1021/ja00833a035

Products guided by the article

Product name:2-methyl-4-benzyloxy-1-naphthol

Cas No:53772-21-7

R&D Labs maybe for 53772-21-7

JIANGXI ZHANGFENG CHEMICAL CO., LTD.

Contact:+86-0799-3413066

Address:Xiyuan village, Xiabu Town, Xiangdong District
Eastar Chemical Corporation

website:http://www.eastarchem.com/

Contact:1-800-898-2436

Address:1215 K Street, STE 1700
Taixing Shenfeng Chemical Co., Ltd.

Contact:+86-523-87117033, 87117666

Address:4# Yinsanlu, Huangqiao town, Taixing, Jiangsu, China.
Shanghai Forever Synthesis Co.,Ltd.

Contact:021-61124658

Address:Zhoukang Road,Pudong New District,Shanghai,China
Xi'an Galaxy Chemicals CO., Ltd

Contact:86-29-89380370

Address:No.8, Gaoxin three road, Xi'an city.

Relevant to this article

A highly efficient and aerobic protocol for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives via a palladium-catalyzed ligand-free Suzuki reaction

Doi:10.1039/c2ob26119g
(2012)
Catalytic Generation of C1 Ammonium Enolates from Halides and CO for Asymmetric Cascade Reactions

Doi:10.1002/anie.201901501
(2019)
One-pot asymmetric synthesis of 2-and 2,3-disubstituted tetrahydrofuran derivatives

Doi:10.1021/jo300414u
(2012)
Synthesis and evaluation of 17α-(dimethylphenyl)vinyl estradiols as probes of the estrogen receptor-α ligand binding domain

Doi:10.1016/j.steroids.2012.01.003
(2012)
Highly orthogonal functionalization of ADMET polymers via photo-induced Diels-Alder reactions

Doi:10.1021/ma3007043
(2012)
A simple metal-free synthesis of 2-substituted pyridine-4,5-dicarboxylates and their N-oxides

Doi:10.1016/j.tet.2012.04.013
(2012)

Article Doi

DOI: 10.1021/ja00833a035