PARTICIPATION OF PERI-HYDROXYL GROUP IN THE TRIFLUOROACETOLYSIS OF NAPHTHALENESULFONAMIDES

DOI: 10.1016/S0040-4039(00)95128-1

Source and publish data:

Tetrahedron Letters p. 6071 - 6074 (1985)

Update date:2022-08-05

Topics:

Authors:

Mazaleyrat, Jean-Paul

Wakselman, Michel

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

Article abstract of DOI:10.1016/S0040-4039(00)95128-1

Trifluoroacetolysis of N-alkyl-8-hydroxy-naphthalenesulfonamides generally leads to the corresponding amines and naphthosultones.A model experiment shows that this reaction may be used in a two-step cleavage of sulfonamide protecting groups.

Full text of DOI:10.1016/S0040-4039(00)95128-1

Products guided by the article

Product name:8-Hydroxy-5,7-dinitro-naphthalene-1-sulfonic acid benzylamide

Cas No:103708-18-5

R&D Labs maybe for 103708-18-5

Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China
Jiangxi Dongbang Pharmaceutical Co., Ltd.

Contact:+86-795-4433603, 4433388

Address:Fengxin Industrial Park, Fengxin County, Jiangxi Province, P.R.C
Shanghai ZaiQi Bio-Tech Co., Ltd.,

Contact:+86-21-5482 4098

Address:Bldg. No.7, No.201 MinYi Rd，Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
Shandong Bolode Bio-Technology Co., LTD

Contact:+86-0531-58966870

Address:136 Jingyi Road,Huaiyin District,Jinan,Shandong,China
enantiotech corporation ltd

Contact:+86-0760-85282375

Address:zhongjing road,zhongshan torch hi-tech industrial development zone

Relevant to this article

Alkylation of aryl 3-oxopropanedithioate and 3-amino-1-aryl-3-thioxo-1-propanones as an effective tool for the construction of differently substituted thiophenes and annulated thiophenes

Doi:10.1016/j.tet.2008.04.036
(2008)
Asymmetric Electrophilic Amination: Synthesis of α-Amino and α-Hydrazino Acids with High Optical Purity

Doi:10.1021/ja00280a049
(1986)
Formation of a hydrogen-bonded barbiturate [2]-rotaxane

Doi:10.1021/ol500099u
(2014)
Synthesis and antibacterial activity of ethyl 2-amino-6-methyl-5-oxo-4- aryl-5,6-dihydro-4H-pyrano[3,2-c]quinoline-3-carboxylate

Doi:10.1016/j.cclet.2013.12.010
(2014)
Intramolecular Homolytic Displacements. 24. Simple Access to Glycidic Esters via Induced Decomposition of Peroxyketals Derived from Ethyl 2-(1-Hydroxyperoxyethyl)propenoate

Doi:10.1021/jo00096a018
(1994)
Screening of a modular sugar-based phosphite-oxazoline ligand library in asymmetric Pd-catalyzed Heck reactions

Doi:10.1002/chem.200601714
(2007)

Article Doi