Synthesis of an indole analog of magallanesine via the [1,2]-Meisenheimer rearrangement

DOI: 10.1002/jhet.5570330658

Source and publish data:

Journal of Heterocyclic Chemistry p. 1909 - 1913 (1996)

Update date:2022-08-05

Topics:

Authors:

Yoneda, Ryuji

Kimura, Tetsuya

Kinomoto, Junko

Harusawa, Shinya

Kurihara, Takushi

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

Article abstract of DOI:10.1002/jhet.5570330658

Ring expansion of azetopyridoindole 11 via the [1,2]-Meisenheimer rearrangement of the corresponding N-oxide 12 gave azocinoindole 14, which was converted into the N-benzoylenaminone 18 in 5 steps. Intramolecular cyclization of 18 was accomplished by a mo

Full text of DOI:10.1002/jhet.5570330658

Products guided by the article

Product name:2-(9-Benzenesulfonyl-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl)-ethanol

Cas No:187272-06-6

R&D Labs maybe for 187272-06-6

Shanghai Maxchemco Chemical Industry Co., Ltd.

Contact:(86)21-51079223

Address:No.1305-8, B241, the Ecust Park, Huajing Road, Xuhui District, Shanghai
Shanghai FWD Chemicals ltd

website:http://www.fwdchem.com

Contact:86-21-54450828

Address:Room 802,Lotus Tower ,159 Tianzhou Road,Xuhui District,Shanghai
SHANDONG QINGYUNCHANGXIN CHEMICAL SCIENCE-TECH CO.,LTD

Contact:86-21-60560171

Address:1689Donghuan Rade,Qingyun County, Dezhou City, Shandong,China
Hangzhou Donglou Bio-nutrient Co., Ltd.

Contact:+86-571-82225795,13967112289

Address:Louta Town, Xiaoshan,Hangzhou,Zhejiang
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China

Relevant to this article

Doi:10.1021/ja01111a045
(1953)
The preparation of racemic and enantiomerically pure myo-inositol derivatives as intermediates for the synthesis of phosphatidylinositol 3-, 3,4-bis-, and 3,4,5-tris-phosphates and for the synthesis of analogues of 1D-myo-inositol 1,3,4,5-tetrakisphosphat

Doi:10.1016/S0008-6215(96)00211-X
(1996)
Evidence for divalent iodine (9-I-2) radical intermediates in the thermolysis of (tert-butylperoxy)iodanes. An unusually efficient deiodination of o-iodocumyl alcohols by cyclohexyl radicals

Doi:10.1021/ja9636404
(1997)
Synthesis of 1-(2-Hydroxyphenyl)-2,4-imidazolidinedione Derivatives through Cyclic Transformations of Ethyl 2-Oxo-3(2H)-benzoxazoleacetate Derivatives

Doi:10.1002/jhet.5570330645
(1996)
ERβ ligands. Part 2: Synthesis and structure-activity relationships of a series of 4-hydroxy-biphenyl-carbaldehyde oxime derivatives

Doi:10.1016/j.bmc.2004.03.028
(2004)
Evidence that steric factors modulate reactivity of tautomeric iron-oxo species in stereospecific alkane C-H hydroxylation

Doi:10.1039/c3cc47830k
(2014)

Article Doi