A Synthesis of Pyrrole Derivatives from O-(2-Hydroxyethyl)-ketoximes

DOI: 10.1039/c39860000903

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 903 - 904 (1986)

Update date:2022-08-02

Topics:

Authors:

Dhanak, Dashyant

Reese, Colin B.

Romana, Sergio

Zappia, Giovanni

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

Article abstract of DOI:10.1039/c39860000903

Acetophenone, cyclohexanone, cycloheptanone, cyclo-octanone, and heptan-4-one were converted, via their O-(2-hydroxyethyl)-oximes <(5), (6a), (6b), (6c), and (8)> into the pyrrole derivatives <(2b), (7a), (7b), (7c) and (9), respectively> in satisfactory overall yields.

Full text of DOI:10.1039/c39860000903

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

View Online

Products guided by the article

Product name:O-(2-hydroxy-ethyl)-cyclohexanone oxime

Cas No:50553-03-2

R&D Labs maybe for 50553-03-2

Afine Chemicals Limited

website:http://www.afinechem.com

Contact:+86-571-85134551

Address:No. 206 Zhen Hua Road, Hangzhou 310030, Zhejiang, China
Kaiping Genuine Biochemical Pharmaceutical Co.,Ltd.

Contact:+86-750-2881198

Address:No.1, Xinke Road, Shatang Town, Kaiping, Guangdong Province, P.R.China
Joyochem Co., Ltd.

website:https://sdjingyuan.lookchem.com/

Contact:86-531-82687998

Address:Factory Building 11, Jinan Comprehensive free trade zone, Shandong, China
Shandong LuZhou Amino Acid Co., Ltd

Contact:86-539-2218025

Address:yishui economic and technical development zone zhenxing south road
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China

Relevant to this article

N-sulfinyl beta-amino Weinreb amides: synthesis of enantiopure beta-amino carbonyl compounds. Asymmetric synthesis of (+)-sedridine and (-)-allosedridine.

Doi:10.1021/ol034119z
(2003)
Doi:10.1021/ja00804a021
(1973)
The synthesis of mono- and difluorinated 2,3-dideoxy-d-glucopyranoses

Doi:10.1016/j.jfluchem.2014.08.023
(2015)
SYNTHESIS OF TETRAPHENYLPORPHINS WITH REACTIVE GROUPS IN THE BENZENE RINGS. 3. USE OF DIAZOTATION FOR THE PREPARATION OF SUBSTITUTED TETRAPHENYLPORPHINS

Doi:10.1007/BF00542778
(1986)
Stereoselective synthesis of epoxyalkyl glycoside precursors of glycosyl glycerol analogues from alkenyl glycosides of N-acetyl-D-glucosamine derivatives

Doi:10.1016/S0957-4166(02)00649-3
(2002)
Crystal and molecular structures of (20R)-20-aminopregn-5-en-3β-ol and (20S)-20-aminopregn-5-en-3β-ol hydrochloride

Doi:10.1023/A:1009553022723
(2000)

Article Doi