Scholarly article on Benzoyl-N-(p-cyanophenyl)carbamoylperoxid 25434-16-6 from Bulletin of the Chemical Society of Japan p. 1981,1982

DOI: 10.1246/bcsj.47.1981

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1981,1982 (1974)

Update date:2022-08-04

Topics:

Authors:

Okazaki Okazaki

Simamura

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

Article abstract of DOI:10.1246/bcsj.47.1981

Full text of DOI:10.1246/bcsj.47.1981

Products guided by the article

Product name:Benzoyl-N-(p-cyanophenyl)carbamoylperoxid

Cas No:25434-16-6

R&D Labs maybe for 25434-16-6

Purestar Chem Enterprise Co.,Ltd

website:http://www.purestarchem.com

Contact:05722157374

Address:no235.huanchengdong Rd
Jinan Trio PharmaTech Co., Ltd

Contact:86-531-88811783；+(0)13153010282

Address:2766 Yingxiu Road, Jinan High-Tech Zone, China
Beijing Chemdow Co., Ltd

website:http://www.chemdow.com

Contact:0086-10-82435335

Address:Room 401,Unit 3,4th Floor,Shangdijiayuan,Shangdi East Road, Haidian District,Beijing
Shandong Shouguang Songchuan Industrial Additives Co.,Ltd

Contact:+86-536-8566856

Address:Shouguang,Shandong,China
Shanghai Yudiao Chemistry Technology Co.,Ltd

Contact:0086-18964703211

Address:Building NO.5, NO.218,Rongtian Road,ganxiang town,Jinshan District,shanghai,201518,china

Relevant to this article

Rhodium-catalyzed asymmetric 1,4-addition to 1-alkenylphosphonates [13]

Doi:10.1021/ja993184u
(1999)
Doi:10.1016/S0889-8545(00)80030-3
()
Synthesis of nitrocarbazole compounds and their electrocatalytic oxidation of alcohol

Doi:10.1016/S1872-2067(15)61047-6
(2016)
[Pd(N,N-chelate)(olefin)] complexes containing chiral nitrogen chelates based on carbohydrates - Enantioselectivity of olefin coordination

Doi:10.1002/(SICI)1099-0682(199911)1999:11<1939::AID-EJIC1939>3.0.CO;2-2
(1999)
Asymmetric synthesis of conformationally constrained 4-hydroxyprolines and their applications to the formal synthesis of (+)-epibatidine

Doi:10.1016/S0957-4166(99)00408-5
(1999)
Stereoselective reactions of N-(9-phenylfluoren-9-yl)-4-oxoproline enolates. An expedient route for the preparation of conformationally restricted amino acid analogues

Doi:10.1021/jo990283h
(1999)

Article Doi

DOI: 10.1246/bcsj.47.1981