Scholarly article on Thioacetic acid S-(2,3,5,6-tetrafluoro-phenyl) ester 107697-58-5 from Journal of the American Chemical Society p. 451 - 464

DOI: 10.1021/ja00444a023

Source and publish data:

Journal of the American Chemical Society p. 451 - 464 (1977)

Update date:2022-08-04

Topics:

Authors:

Hupe,D.J.

Jencks,W.P.

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

Article abstract of DOI:10.1021/ja00444a023

Full text of DOI:10.1021/ja00444a023

Products guided by the article

Product name:Thioacetic acid S-(2,3,5,6-tetrafluoro-phenyl) ester

Cas No:107697-58-5

R&D Labs maybe for 107697-58-5

HANGZHOU FOREWIN PHARMA CO., LTD

Contact:+86-571-89053961

Address:hangzhou
Zipont chem(wuhan）Tech co.，Ltd

Contact:+86-27-87587198

Address:wuhan
Anhui New Star Pharmaceutical Development Co., Ltd

Contact:013956922763

Address:Floor 3, F9A, F Workshop, No.110 Kexue Road, High-Tech Development Zone, Hefei, Anhui ,China
ALPHA PHARMACEUTICAL CO，LTD JIANGSU

Contact:+86-527-84829968,+86-527-84829998

Address:suqian city
TIANJIN NORTH JINHENG CHEMICAL PLANT.

Contact:0086-22-59952083

Address:DongShigu Country In JiXian TianJin China

Relevant to this article

Synthesis of (+)-(2S,6S)-trans-α-Irone and of (-)-(2S,6S)-trans-γ-Irone

Doi:10.1002/hlca.19890720713
(1989)
Synthesis of N-<(1R)-(1,5/4,6)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexenyl> derivatives of 4'-amino-4'-deoxy- and 4'-amino-4',6'-dideoxy-cellobiose

Doi:10.1016/S0008-6215(00)90121-6
(1986)
Estimation of heterogeneous rate constants of reaction of electrochemically generated o-benzoquinones with various nucleophiles containing thiol group

Doi:10.1002/kin.20402
(2009)
A 'click' chemistry route to 'capped' porphyrins

Doi:10.1055/s-2008-1077899
(2008)
9-CIS AND 11-CIS ISOMERS OF 18,18,18-, 19,19,19- AND 20,20,20-TRIFLUORORETINAL

Doi:10.1016/S0040-4039(00)95701-0
(1987)
Synthesis, biological evaluation and molecular modelling of 2′-hydroxychalcones as acetylcholinesterase inhibitors

Doi:10.3390/molecules21070955
(2016)

Article Doi

DOI: 10.1021/ja00444a023