Scholarly article on 1,4-bis-acetoxymethyl-cyclohexene 107153-75-3 from Journal of the American Chemical Society p. 5393,5395

DOI: 10.1021/ja01529a035

Source and publish data:

Journal of the American Chemical Society p. 5393,5395 (1959)

Update date:2022-08-03

Topics:

Authors:

Bailey Bailey

Barclay Barclay

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

Article abstract of DOI:10.1021/ja01529a035

Full text of DOI:10.1021/ja01529a035

Products guided by the article

Product name:1,4-bis-acetoxymethyl-cyclohexene

Cas No:107153-75-3

R&D Labs maybe for 107153-75-3

Zibo Fuxi'er Chemical Co.,Ltd （Shanxian Fuxi'er Chemical Co.,Ltd）

Contact:+86-533-2091422

Address:Eastern 4 on the 3th Road ,Liangxiang Industrial Park, Zibo city ,Shandong,China
King Brother Chem Co., Ltd

website:http://www.uvchemkeys.com

Contact:0086-021-58785816

Address:RM2607 Building No.1 Guosheng, Lane 388, Zhongjiang Road, Putuo District, Shanghai 200062 China
Shijiazhuang Haotian Chemical Co., Ltd.

Contact:86-311-85044374

Address:293 Donggang Road
Onlychem (Jinan)Biotech Co.,Ltd

Contact:86-531-83175885

Address:No. 44, Honglou South Road, Jinan,China
Taizhou Elitechemie MediPharma Technology Co.,Ltd.

Contact:+86-523-86810021

Address:Building G14,NO.1 Avenue,China Medical City, Taizhou, Jiangsu,China

Relevant to this article

Selective biocatalytic deacylation studies on furanose triesters: A novel and efficient approach towards bicyclonucleosides

Doi:10.1039/b711455a
(2007)
Doi:10.1016/S0022-1139(00)80969-0
(1984)
Sequential copper-catalyzed vinylation/ cyclization: An efficient synthesis of functionalized oxazoles

Doi:10.1021/ol7024718
(2007)
Enhancing Insulated Conjugated Polymer Fluorescence Quenching by Incorporating Dithia[3.3]paracyclophanes

Doi:10.1021/acs.macromol.1c00136
(2021)
Synthesis, X-ray, and electronic structures of a new nickel dibromide complex. Activity in the regioselective catalyzed dimerization of ethylene into 1-butene

Doi:10.1021/ic701529a
(2007)
Synthesis of C-glycosyl phosphonate derivatives of 4-amino-4-deoxy-α-L-arabinose

Doi:10.3762/bjoc.16.2
(2020)

Article Doi

DOI: 10.1021/ja01529a035