Regioselective acylation of benzoselenazolinone

DOI: 10.1080/00397919308009820

Source and publish data:

Synthetic Communications p. 621 - 629 (1993)

Update date:2022-09-26

Topics:

Authors:

Galet Galet

Vaccher Vaccher

Bernier Bernier

Henichart

Lesieur Lesieur

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

Article abstract of DOI:10.1080/00397919308009820

Substitutions on benzoselenazolinone were performed by using successively (i) aliphatic or aromatic acids and (ii) acid chlorides in the presence of (i) polyphosphoric acid and (ii) aluminium chloride in dimethylformamide. Regioselective acylation at C₆ position was demonstrated by ¹H NMR using Nuclear Overhauser Effect.

Full text of DOI:10.1080/00397919308009820

Synthetic Communications

ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20

Regioselective Acylation of Benzoselenazolinone

V. Galet , M. P. Vaccher , J. L. Bernier , J. P. Henichart & D. Lesieur

To cite this article: V. Galet , M. P. Vaccher , J. L. Bernier , J. P. Henichart & D. Lesieur (1993)

Regioselective Acylation of Benzoselenazolinone, Synthetic Communications, 23:5, 621-629,

DOI: 10.1080/00397919308009820

To link to this article: http://dx.doi.org/10.1080/00397919308009820

Published online: 27 Oct 2006.

Submit your article to this journal

Article views: 1

View related articles

Citing articles: 4 View citing articles

Full Terms & Conditions of access and use can be found at

http://www.tandfonline.com/action/journalInformation?journalCode=lsyc20

Download by: [Universite Laval]

Date: 21 September 2015, At: 08:15

Products guided by the article

Product name:6-Benzoyl-3-methyl-3H-benzoselenazol-2-one

Cas No:142776-27-0

R&D Labs maybe for 142776-27-0

Zhenjiang Haitong Chemical Industry Co., Ltd.

Contact:+86 (511) 8448-0369

Address:Baoyan Town, Dantu District, Zhenjiang City, Jiangsu, China
Suzhou HeChuang Chemical Co.,Ltd.

Contact:+86-512-88800520

Address:No.9 Guanchao Rd,Changshu Advanced Materials Industy Park
Hebei Think-Do Environment Co., Ltd

website:http://www.thinkdo-environment.com

Contact:0311-86510809

Address:No 6, Shilian Middle Street, Circular Chemical Industry Park
Daicel Chiral Technologies (China)CO.,LTD

Contact:021-5046-0086*8

Address:Part C, FL 5, the 16th Building, No. 69, XiYa Road, WaiGaoQiao Free Trade Zone, Shanghai, 200131, P.R.China
Nanjing yieldpharma co.ltd

Contact:13813902930 025-52714267

Address:20 Fengji Road, Yuhua Economic Development Zone, Nanjing, Jiangsu, P. R. China

Relevant to this article

Pd-catalyzed C3-selective arylation of pyridines with phenyl tosylates

Doi:10.1039/c3cc41066h
(2013)
Synthesis of 2,5-bis(hetero)aryl 4′-substituted 4,5′- bisoxazoles via copper(I)-catalyzed domino reactions of activated methylene isocyanides with 2-phenyl- and 2-(2-thienyl)-4-[(aryl/heteroaryl)(methylthio) methylene]oxazol-5(4 H)-ones

Doi:10.1021/jo400317g
(2013)
Novel inhibitors of bacterial virulence: Development of 5,6-dihydrobenzo[h]quinazolin-4(3H)-ones for the inhibition of group A streptococcal streptokinase expression

Doi:10.1016/j.bmc.2013.01.046
(2013)
Structure-property relationship of different electron donors: Novel organic sensitizers based on fused dithienothiophene π-conjugated linker for high efficiency dye-sensitized solar cells

Doi:10.1016/j.tet.2013.02.058
(2013)
Asymmetric aldol approach to dibenzylbutyrolactone lignans: Synthesis of (-)-(7′S)-hydroxymatairesinol and (-)-(7′S)-hydroxyarctigenin

Doi:10.1016/j.tetlet.2013.02.044
(2013)
The behavior of pyrrolyl ligands within the rare-earth metal alkyl complexes. Insertion of CN and CO double bonds into Ln-σ-C bonds

Doi:10.1039/b926038b
(2010)

Article Doi