Scholarly article on 2H-2,6-dimethylphenol 22100-62-5 from Journal of the American Chemical Society p. 228,229

DOI: 10.1021/ja01534a058

Source and publish data:

Journal of the American Chemical Society p. 228,229 (1958)

Update date:2022-08-03

Topics:

Authors:

Walling Walling

Hodgdon Hodgdon

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

Article abstract of DOI:10.1021/ja01534a058

Full text of DOI:10.1021/ja01534a058

Products guided by the article

Product name:²H-2,6-dimethylphenol

Cas No:22100-62-5

R&D Labs maybe for 22100-62-5

Jiangsu Willing Bio-Tech Co ltd

website:http://www.willingbio.com/

Contact:+86 18796908173

Address:No 18 Guoqiao Road
Hangzhou innopharma technology Co,.Ltd.(expird)

Contact:+86-13388601988

Address:Room845,lixin building, moganshan road, hangzhou, china
Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
Puyang Willing Chemicals Co.,Ltd.

Contact:86-393-4840366

Address:Puyang Henan China
Shanghai Standard Biotech Co., Ltd.

Contact:+86-18502101150

Address:Room 103, Building 2nd, NO.720, Cailun Road , Pudong District, Shanghai, China

Relevant to this article

Total synthesis of a-tetracyclic anti-tumor, UCE6

Doi:10.7164/antibiotics.55.1076
(2002)
A novel donor for stereoselective α-Sialylation; efficient synthesis of an α(2-8)-linked bis-sialic acid unit

Doi:10.1016/S0040-4039(99)00175-6
(1999)
Cobalt-mediated Mizoroki-Heck-type reaction of epoxide with styrene

Doi:10.1002/adsc.200404074
(2004)
LINEAR TETRAPYRROLIC INTERMEDIATES FOR BIOSYNTHESIS OF THE NATURAL PORPHYRINS. EXPERIMENTS WITH MODIFIED SUBSTRATES.

Doi:10.1016/S0040-4020(01)88706-8
(1983)
Allylic amination of internal alkynes with aromatic and aliphatic amines using polymer-supported triphenylphosphane-palladium complex as a heterogeneous and recyclable catalyst

Doi:10.1002/ejoc.201000463
(2010)
Synthesis of trifluoroalkyl- and fluoroaryl-substituted 4,5-dihydro-1H-1,2,4-triazole-5-thiones

Doi:10.1023/B:RUJO.0000044552.07729.40
(2004)

Article Doi

DOI: 10.1021/ja01534a058