Scholarly article on 4,5-dihydrophenanthro[3,4-c]furan-1,3-dione 7512-19-8 from Journal of the American Chemical Society p. 1851,1853

DOI: 10.1021/ja01313a027

Source and publish data:

Journal of the American Chemical Society p. 1851,1853 (1935)

Update date:2022-07-28

Topics:

Authors:

Fieser Fieser

Hershberg

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

Article abstract of DOI:10.1021/ja01313a027

Full text of DOI:10.1021/ja01313a027

Products guided by the article

Product name:4,5-dihydrophenanthro[3,4-c]furan-1,3-dione

Cas No:7512-19-8

R&D Labs maybe for 7512-19-8

Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
Zhejiang Newfine Industry Co.,Ltd.

Contact:+86-573-82262042

Address:No.225,Dongqing Road, garoms@163.com
GN chemicals co.,ltd

Contact:86 311 85902108 / 85902109

Address:room 1001-1005 ,huanghe Road ,shijiazhuang ,China
Shanghai Hanshare Industry Co.,Ltd.

Contact:86 21 20960688

Address:RM902-903,Building E, Wanda Plaza,No.26,Zhoukang Road, Pudong District, Shanghai, China
JiangXi Keyuan Biopharma Co., LTD.

Contact:+86-563-6833666

Address:Guangde Fine Chemical Zone, Anhui Province, China

Relevant to this article

Engineered Artificial Carboligases Facilitate Regioselective Preparation of Enantioenriched Aldol Adducts

Doi:10.1021/jacs.0c02351
(2020)
Nuclear magnetic resonance and mass spectra of organomercury hydrides and deuterides

Doi:10.1039/dt9960000153
(1996)
Copper-promoted Chan-Lam coupling between enaminones and aryl boronic acids

Doi:10.1016/j.tetlet.2018.10.030
(2018)
Nazarov cyclization of divinyl ketones bearing an ester group at the β-position: A remarkable effect of α-substitution and alkene geometry on regioselectivity

Doi:10.1039/c6ob00081a
(2016)
Studies on the Synthesis of Chemotherapeutics. 10. Synthesis and Antitumor Activity of N-Acyl- and N-(Alkoxycarbonyl)-5-fluorouracil Derivatives

Doi:10.1021/jm00186a008
(1980)
Design, synthesis and antitubercular evaluation of benzothiazinones containing a piperidine moiety

Doi:10.1016/j.ejmech.2018.03.060
(2018)

Article Doi

DOI: 10.1021/ja01313a027