CHEMISTRY OF O-ARYLHYDROXYLAMINES. A NOVEL ACID-CATALYZED REARRANGEMENT OF O-ARYL-N-ACETOACETYLHYDROXYLAMINES TO BENZOFURANS

DOI: 10.1016/S0040-4039(00)84951-5

Source and publish data:

Tetrahedron Letters p. 4209 - 4212 (1986)

Update date:2022-08-04

Topics:

Authors:

Endo, Yasuyuki

Namikawa, Kohshi

Shudo, Koichi

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

Article abstract of DOI:10.1016/S0040-4039(00)84951-5

Acid-catalyzed rearangement of O-aryl-N-acetoacetylhydroxylamines (1) affords 2-methylbenzofuran-3-carboxamides.Some abnormal rearrangements of the title compounds are also described.

Full text of DOI:10.1016/S0040-4039(00)84951-5

Products guided by the article

Product name:3-(2-actoacetamido)-2,6-xylenol

Cas No:107449-11-6

R&D Labs maybe for 107449-11-6

Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
Weihao Chemtech (ChangZhou) Co., Ltd.(expird)

Contact:051989185693

Address:NO 217 huangshan Rd ,Changzhou
Phytomarker Ltd.(expird)

Contact:+86-22-26358246

Address:601-4-20, Fujiayuan, Tiantai Road, Hebei District, Tianjin, China
Nanyang Tianhua pharmaceutical Co.,Ltd.

Contact:+8618639816203

Address:Longsheng Industrial Park
Shanghai doly chemical Co.,Ltd

Contact:+86-21-34716221

Address:No.328,WuHe Roard,MinHang,ShangHai China

Relevant to this article

Doi:10.1021/jo00883a012
(1976)
Asymmetric hetero diels-alder reaction of nitroso compounds utilizing tartaric acid ester as a chiral auxiliary

Doi:10.3987/COM-08-S(N)94
(2008)
Synthesis and characterization of 5-substituted novel isoxazolidines derived from 1,3-dipolar cycloaddition of nitrones with olefins: Studies of antibacterial and antifungal activities

Doi:10.1081/SCC-120018773
(2003)
Unusual reaction of N-aroyldihydrocyclopenta-pyrazolidinol with ketenes: Formation of 1,3,4-oxadiazoles

Doi:10.1016/S0040-4020(03)00633-1
(2003)
Doi:10.1021/ac50003a030
(1976)
Novel synthetic approach to the 8,10-dimethyl anti-syn-anti-perhydrophenanthrene skeleton

Doi:10.1021/ol034213f
(2003)

Article Doi