ONE-POT SYNTHESIS OF α-CHLORONITRILES FROM ARYLCARBONYL COMPOUNDS

DOI: 10.1246/cl.1984.1979

Source and publish data:

Chemistry Letters p. 1979 - 1980 (1984)

Update date:2022-08-02

Topics:

Authors:

Kiyooka, Syun-ichi

Fujiyama, Ryoji

Kawaguchi, Katsuhiko

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

Article abstract of DOI:10.1246/cl.1984.1979

α-Chloronitriles are prepared by the reaction of arylcarbonyl compounds and trimethylsilyl cyanide with a stoichiometric amount of titanium tetrachloride in good yields.

Full text of DOI:10.1246/cl.1984.1979

Products guided by the article

Product name:2-Chloro-2-p-tolyl-propionitrile

Cas No:94083-87-1

R&D Labs maybe for 94083-87-1

ZHEJIANG SYNOSE TECH CO.,LTD.

website:https://www.synose.com/

Contact:86-579-82275537

Address:No.1958 Liyu Road , jinhua,zhejiang,China
Hangzhou Ledun Technology Co.,Ltd.

Contact:86-571-18767088918

Address:No.6 street,XiaSha,Hangzhou,China.
Zhejiang kehong chemical co., ltd

Contact:0086-575-85522000

Address:xiner center RD binhai industrial zone shaoxing zhejiang province P.R.China,312073
SHIFANG SUHONG CHEMICAL CO.,LTD

Contact:+86-838-2224563

Address:Room 1207 Zongchen Sunshine No.128 Taishan South Road,Deyang City,Sichuan China
zonk drug r&d limited

Contact:+86-20-32051076

Address:1105,Building A, International Business Incubator,Science City

Relevant to this article

Doi:10.1021/jm01240a015
(1962)
Tanjungides a and B: New antitumoral bromoindole derived compounds from Diazona cf formosa. isolation and total synthesis

Doi:10.3390/md12021116
(2014)
O-glycoside orientation is an essential aspect of base J recognition by the kinetoplastid DNA-binding protein JBP1

Doi:10.1002/anie.200604635
(2007)
Electrospray ionization and collision induced dissociation mass spectrometry of primary fatty acid amides

Doi:10.1021/ac203158u
(2012)
The Determination of Small Amounts of Enantiomeric Impurities in α-Halo Carboxylic Acids

Doi:10.1055/s-1987-27896
(1987)
A highly efficient azide-based protecting group for amines and alcohols

Doi:10.1021/ol0707160
(2007)

Article Doi