A Short Efficient Route to Acronycine and Other Acridones

DOI: 10.1039/c39910001046

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1046 - 1048 (1991)

Update date:2022-08-04

Topics:

Authors:

Horne, Stephen

Rodrigo, Russell

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

Article abstract of DOI:10.1039/c39910001046

A Fries type rearrangement of N-tosyl-o-iodobenzanilides, triggered by lithium-iodine exchange at low temperature is the key step in a general, regiospecific synthesis of acridones.

Full text of DOI:10.1039/c39910001046

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

View Article Online

Products guided by the article

Product name:N-(2-Fluoro-6-methoxy-benzoyl)-N-(2-iodo-phenyl)-4-methyl-benzenesulfonamide

Cas No:136138-34-6

R&D Labs maybe for 136138-34-6

Suzhou Chiral Pharmaceuticals Co., Ltd.

Contact:86-0512-63197058

Address:Building A, No. 2358, Chang'an Road, Wujiang Science Park
Watson International Ltd

Contact:+44 (0)2036089360-31

Address:Chanceryhouse,Chancery Lan
ShangHai BMG Chemical Co., Ltd

Contact:+86-13524845543

Address:Room 602, no 291 sikai road shanghai
Tianjin Hedong Red Cliff Chemical Reagent Factory

Contact:+86-022-84780548

Address:Li Ming Zhuang Gong Ye Yuan,Dongli District,Tianjin,China
Anhui Hope-Chem Co., Ltd.

Contact:86-551-63540590

Address:No 1388 Furong Rd., Hefei, Anhui, China

Relevant to this article

Structure-activity relationships in group 3 metal catalysts for asymmetric intramolecular alkene hydroamination. An investigation of ligands based on the axially chiral 1,1′-binaphthyl-2,2′-diamine motif

Doi:10.1039/c1dt10222b
(2011)
Enantiodivergent Synthesis of Tertiary α-Aryl 1-Indanones: Evidence Toward Disparate Mechanisms in the Palladium-Catalyzed Decarboxylative Asymmetric Protonation

Doi:10.1021/acs.joc.7b00303
(2017)
Isomerization and ring-closing metathesis for the synthesis of 6-, 7- and 8-membered benzo- and pyrido-fused N,N-, N,O- and N,S-heterocycles

Doi:10.1016/j.tetlet.2004.10.108
(2004)
POSSIBLE REACTION PATHWAYS FOR THE FORMATION OF 3-CHLORO-4-(DICHLOROMETHYL)-5-HYDROXY-2(5H)-FURANONE (MX).

Doi:10.1016/0045-6535(94)90329-8
(1994)
Rhodium-catalyzed enantioselective reductive aldol reaction [11]

Doi:10.1021/ja9944453
(2000)
Synthesis of some basic 3-(1-acylaminobenzyl)-2H-1-benzopyran-2-ones

Doi:10.1002/ardp.2503240804
(1991)

Article Doi