A Facile Displacement of Tertiary Nitro Group by Hydrogen with Sodium Hydrogentelluride

DOI: 10.1246/bcsj.58.1067

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1067 - 1068 (1985)

Update date:2022-08-11

Topics:

Authors:

Suzuki, Hitomi

Takaoka, Koji

Osuka, Atsuhiro

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

Article abstract of DOI:10.1246/bcsj.58.1067

Sodium hydrogentelluride is a useful reagent for replacement of a class of tertiary nitro group by hydrogen.

Full text of DOI:10.1246/bcsj.58.1067

Products guided by the article

Product name:4-ISOPROPYLBENZONITRILE

Cas No:13816-33-6

R&D Labs maybe for 13816-33-6

Suzhou Credit International Trading Co., Ltd

Contact:+86-512-65398039

Address:Qingdeng, Hightech. District, Suzhou
Luoyang Aoda chemical Co.,Ltd.

Contact:+86-379-67518785 67516588

Address:MiaoWan industry district,YanShi City,Henan,China
Jinan Jianfeng Chemical Co., Ltd

Contact:0086-531-88110457

Address:sales01(-a-t-)pharmachemm{dot}c+o+m
ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Joyochem Co., Ltd.

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

Contact:86-531-82687998

Address:Factory Building 11, Jinan Comprehensive free trade zone, Shandong, China

Relevant to this article

Effect of chemical composition of Sr_xCa_{1 - X}Fe ₂O₄ (0.0)

Doi:10.1016/j.apcata.2014.03.040
(2014)
Efficient chemical fixation of CO₂ into cyclic carbonates using poly(4-vinylpyridine) supported iodine as an eco-friendly and reusable heterogeneous catalyst

Doi:10.1002/hc.21440
(2018)
Thiocyanation of α-amino carbonyl compounds for the synthesis of aromatic thiocyanates

Doi:10.1177/1747519820923553
(2021)
An approach for continuous-flow processing of reactions that involve the in situ formation of organic products

Doi:10.1016/j.tetlet.2010.11.027
(2011)
Doi:10.1063/1.1743543
(1957)
Reactions of Azolium Cations. II. Regioselective N2 Alkylation of 5-Aryltetrazoles with Isopropyl Alcohol in Sulfuric Acid Media: Effect of Electronic Properties of Aryl Substituents on the Reaction Rate

Doi:10.1002/kin.550270908
(1995)

Article Doi