Regioselective synthesis of 8-hydroxytetrahydroquinolines by the cyclization of m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes

Ayako Ono; Katsuya Uchiyama; Yujiro Hayashi; Koichi Narasaka

doi:10.1246/cl.1998.437

Regioselective synthesis of 8-hydroxytetrahydroquinolines by the cyclization of m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes

Ayako Ono, Katsuya Uchiyama, Yujiro Hayashi, Koichi Narasaka

Research output: Contribution to journal › Article › peer-review

22 Citations (Scopus)

Abstract

8-Hydroxy-1,2,3,4-tetrahydroquinolines are synthesized from m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes by the cyclization on the sp² nitrogen atom of the oxime derivatives using sodium hydride and sodium cyanoborohydride.

Original language	English
Pages (from-to)	437-438
Number of pages	2
Journal	Chemistry Letters
Issue number	5
DOIs	https://doi.org/10.1246/cl.1998.437
Publication status	Published - 1998 Jan 1
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

Access to Document

10.1246/cl.1998.437

Cite this

@article{e429fedf5a784500b789ca6d4308645d,

title = "Regioselective synthesis of 8-hydroxytetrahydroquinolines by the cyclization of m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes",

abstract = "8-Hydroxy-1,2,3,4-tetrahydroquinolines are synthesized from m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes by the cyclization on the sp2 nitrogen atom of the oxime derivatives using sodium hydride and sodium cyanoborohydride.",

author = "Ayako Ono and Katsuya Uchiyama and Yujiro Hayashi and Koichi Narasaka",

year = "1998",

month = jan,

day = "1",

doi = "10.1246/cl.1998.437",

language = "English",

pages = "437--438",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Chemical Society of Japan",

number = "5",

}

TY - JOUR

T1 - Regioselective synthesis of 8-hydroxytetrahydroquinolines by the cyclization of m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes

AU - Ono, Ayako

AU - Uchiyama, Katsuya

AU - Hayashi, Yujiro

AU - Narasaka, Koichi

PY - 1998/1/1

Y1 - 1998/1/1

N2 - 8-Hydroxy-1,2,3,4-tetrahydroquinolines are synthesized from m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes by the cyclization on the sp2 nitrogen atom of the oxime derivatives using sodium hydride and sodium cyanoborohydride.

AB - 8-Hydroxy-1,2,3,4-tetrahydroquinolines are synthesized from m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes by the cyclization on the sp2 nitrogen atom of the oxime derivatives using sodium hydride and sodium cyanoborohydride.

UR - http://www.scopus.com/inward/record.url?scp=0032389290&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032389290&partnerID=8YFLogxK

U2 - 10.1246/cl.1998.437

DO - 10.1246/cl.1998.437

M3 - Article

AN - SCOPUS:0032389290

SN - 0366-7022

SP - 437

EP - 438

JO - Chemistry Letters

JF - Chemistry Letters

IS - 5

ER -

Regioselective synthesis of 8-hydroxytetrahydroquinolines by the cyclization of m-hydroxyphenethyl ketone O-2,4-dinitrophenyloximes

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this