Scholarly article on 2-(3-methoxy-phenethyl)-3-oxo-heptanedioic acid diethyl ester 855897-15-3 from Journal of the American Chemical Society p. 1922,1924

DOI: 10.1021/ja01174a007

Source and publish data:

Journal of the American Chemical Society p. 1922,1924 (1949)

Update date:2022-08-05

Topics:

Authors:

Hunter Hunter

Hogg Hogg

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

Article abstract of DOI:10.1021/ja01174a007

Full text of DOI:10.1021/ja01174a007

Products guided by the article

Product name:2-(3-methoxy-phenethyl)-3-oxo-heptanedioic acid diethyl ester

Cas No:855897-15-3

R&D Labs maybe for 855897-15-3

Longhui qunfeng Chemical Co., Ltd

Contact:86-731-82173407

Address:South-east Industrial Park, Longhui County, Hunan Province, China
Chongqing Yawei Fine Chemical Co.,Ltd

Contact:0086-23-62849407

Address:Ziyou village, Nanquan town, Banan district, Chongqing China
Beijing Wisdom Chemicals Co., Ltd.

Contact:+86-10-52350335

Address:F2, BLDG 19, Liando Valley U, Majuqiao, Tongzhou District, Beijing, China
Cangzhou Senary Chemical Science-tech Co., Ltd

Contact:+86-317-3563899, 3563699

Address:168 Jinde Road, Cangzhou, Hebei, China
Weifang Yukai Chemical Co.,Ltd.

website:http://www.yukaichem.com/en.html

Contact:+86-536-8865336

Address:binhai economic development zone，262737 shangdong，china

Relevant to this article

REACTIONS OF α-HETEROATOM-SUBSTITUTED ETHERS AND SULFIDES WITH SILYL ENOL ETHERS. CHEMOSELECTIVITY IN THE CLEAVAGE OF HETEROATOM-CARBON BONDS BY IODOTRIMETHYLSILANE AND TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE

Doi:10.1246/cl.1983.405
(1983)
A novel synthesis of fused imidazo[5,1-c]-1,2,4-triazoles

Doi:10.1002/jhet.5570200139
(1983)
Rearrangement of the intermediate 1,4-biradicals in photocycloaddition of cyclohex-2-enones to alkenes

Doi:10.1007/BF02496171
(1999)
Synthesis of 35S-labelled arylsulphates byintact animals and by tissue preparations, with particular reference to L-tyrosine O-sulphate.

Doi:10.1042/bj0730723
(1959)
Enantioselective construction of tetrasubstituted stereogenic carbons through bronsted base catalyzed michael reactions: α′-hydroxy enones as key enoate equivalent

Doi:10.1021/ja510603w
(2014)
Doi:10.1021/ja01337a049
(1933)

Article Doi

DOI: 10.1021/ja01174a007

Source and publish data: