Scholarly article on Phenol, 3-[[(2,2-diethoxyethyl)imino]methyl]- 143247-61-4 from Journal of the American Chemical Society p. 860,869

DOI: 10.1021/ja01221a051

Source and publish data:

Journal of the American Chemical Society p. 860,869 (1945)

Update date:2022-08-04

Topics:

Authors:

Woodward

Doering Doering

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

Article abstract of DOI:10.1021/ja01221a051

Full text of DOI:10.1021/ja01221a051

Products guided by the article

Product name:Phenol, 3-[[(2,2-diethoxyethyl)imino]methyl]-

Cas No:143247-61-4

R&D Labs maybe for 143247-61-4

Hangzhou Cherry Pharmaceutical Technology Co., Ltd.

Contact:+86 (571) 8163-6070 / +86 18042403330

Address:262Wangtang Road
QINGDAO ON-BILLION INDUSTRAIL CO.,LTD

website:http://www.obn.com.cn

Contact:+86-15005320811 +86-532-80681989

Address:F35 Parkson Mansion No.44-60 Zhongshan Rd.
ShangHai Original Economy-Trade Develop Co.,Ltd.,

Contact:86-21-68552131

Address:shanghai
NINGXIA DARONG CHEMICALS & METALLURGY CO.,LTD.

Contact:86-952-2179751

Address:Darong Road, Dawukou, Shizuishan, Ningxia 753001, China
Sarchem Laboratories, Inc.

Contact:732.938.2777

Address:5012 Industrial Road Farmingdale, NJ 07727

Relevant to this article

Facile construction of structurally diverse thiazolidinedione-derived compounds via divergent stereoselective cascade organocatalysis and their biological exploratory studies

Doi:10.1021/co400022r
(2013)
Mild and selective base-free C-H arylation of heteroarenes: experiment and computation

Doi:10.1039/c6sc02595a
(2017)
Stereoselective synthesis of α-glycosyl azides by TMSOTf-mediated ring opening of 1,6-anhydro sugars

Doi:10.1002/ejoc.201201580
(2013)
A redox economical synthesis of bioactive 6,12-guaianolides

Doi:10.1021/ol400904y
(2013)
Gold-catalyzed reactions between alkenyldiazo carbonyl species and acetals

Doi:10.1021/jo400419d
(2013)
Synthesis, cytotoxicity, hypolipidemic and anti-inflammatory activities of amine-boranes and esters of boron analogues of choline and thiocholine

Doi:10.1002/jps.2600810514
(1992)

Article Doi

DOI: 10.1021/ja01221a051

Source and publish data: