Scholarly article on 7-(2,4-Bis-benzyloxy-6-methyl-phenyl)-3,5,7-trioxo-heptanoic acid methyl ester 38071-44-2 from Journal of the Chemical Society. Chemical communications p. 953

DOI: 10.1039/C3972000953b

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 953 (1972)

Update date:2022-08-05

Topics:

Authors:

Hay Hay

Harris Harris

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

Article abstract of DOI:10.1039/C3972000953b

Full text of DOI:10.1039/C3972000953b

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:7-(2,4-Bis-benzyloxy-6-methyl-phenyl)-3,5,7-trioxo-heptanoic acid methyl ester

Cas No:38071-44-2

R&D Labs maybe for 38071-44-2

Huayi Isotopes Co.

Contact:+ 86 512 52491118

Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China
Changsha Yonta Industry Co., Ltd.

Contact:+ 86-731-8535 2228

Address:Rm.1717, North Bldg., No.368, East 2nd Ring Road(2nd Section)
Hangzhou Donglou Bio-nutrient Co., Ltd.

Contact:+86-571-82225795,13967112289

Address:Louta Town, Xiaoshan,Hangzhou,Zhejiang
MiHecb Bio-Tech Co., Ltd.

Contact:+86-0592 5353131

Address:No.56 Guani Road Software Park 2,Siming District
Tangshan Wisdom Trading Co.,Ltd

Contact:86 315 2222979

Address:No.41 BeiXinXi Road, Yangguang building 1-1102 , Tangshan, Hebei, China

Relevant to this article

Doi:10.1021/ja01079a011
(1965)
Doi:10.1139/v72-328
(1972)
Oxiranes in the Ritter reaction. Synthesis of 6,7- and 5,8-dimethoxy-3,3-dialkyl-3,4-dihydroisoquinolines by a tandem alkylation-cyclization reaction

Doi:10.1023/A:1017643703041
(2001)
Polyfunctional (R)-2-Hydroxycarboxylic Acids by Reduction of 2-Oxo Acids with Hydrogen Gas or Formate and Resting Cells of Proteus vulgaris

Doi:10.1016/S0040-4020(01)86506-6
(1991)
The photo-Wallach rearrangement. Heavy-atom kinetic isotope effects and mechanism

Doi:10.1139/v86-186
(1986)
Sustainable organophosphorus-catalysed Staudinger reduction

Doi:10.1039/c8gc02136h
(2018)

Article Doi

DOI: 10.1039/C3972000953b