Scholarly article on perfluoro(2-aza-2-pentene) 680-23-9 from Journal of the Chemical Society C: Organic p. 398 - 405

DOI: 10.1039/j39680000398

Source and publish data:

Journal of the Chemical Society C: Organic p. 398 - 405 (1968)

Update date:2022-08-04

Topics:

Authors:

Haszeldine,R.N.

Tipping,A.E.

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

Article abstract of DOI:10.1039/j39680000398

Full text of DOI:10.1039/j39680000398

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

View Article Online

Products guided by the article

Product name:perfluoro(2-aza-2-pentene)

Cas No:680-23-9

R&D Labs maybe for 680-23-9

Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China
Shijiazhuang City Xiehe Pharmaceutical Co., Ltd

Contact:+86-311-80817929

Address:Shangzhuang,Shijiazhuang,China
SPE Chemicals Co.,Ltd

Contact:

Address:ROOM 1715, No#345 Jin Xiang Road, Pudong District
Anhui Dexinjia Biopharm Co., Ltd

Contact:+86-531-82375818

Address:9 Hexie Road, kaifaqu, Taihe
Guangzhou PI & PI Biotech Inc. Ltd.

Contact:+86-20-81716320

Address:13th Floor, Xinbao Technology Industrial Park, No. 2 Ruixiang Road, Huangpu District, Guangzhou,Guangdong,China

Relevant to this article

Nazarov cyclization of 1,4-pentadien-3-ols: Preparation of cyclopenta[b]indoles and spiro[indene-1,4′-quinoline]s

Doi:10.1039/c5cc08596a
(2016)
An Unprecedented Pd-Catalyzed Carbonylative Route to Fused Furo[3,4-b]indol-1-ones

Doi:10.1002/chem.201706067
(2018)
Synthesis of pyrrolo[1,2-a]benzo[f]indole derivatives.

Doi:10.1016/S0040-4039(00)71558-9
(1967)
Palladium(II) complexes with aminomethylphosphine ligands as catalysts for the heck reaction

Doi:10.1002/hc.21038
(2012)
Oxidation of α-trifluoromethyl alcohols using a recyclable oxoammonium salt

Doi:10.1021/jo301477s
(2012)
Choice of Manganese(III) Complexes for the Synthesis of 4,4'-Biphenyldiols and 4,4'-Diphenoquinones

Doi:10.1246/bcsj.65.620
(1992)

Article Doi

DOI: 10.1039/j39680000398