ChemInform

Journal Information
ISSN / EISSN : 0931-7597 / 1522-2667
Published by: Wiley (10.1002)
Total articles ≅ 486,085
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SHERPA/ROMEO
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Latest articles in this journal

Hongyuan Zhao, Wei Han
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652138

Abstract:
In contrast to traditional metal-based oxidative systems the developed homo-coupling of aryl boronic acids or potassium aryltrifluoroborates uses molecular oxygen or iodine as the oxidant, respectively.
Jia Yang, Jing Xiao, Tieqiao Chen, Li-Biao Han
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652375

Jin‐Shun Lin, Xiao-Yang Dong, Tao-Tao Li, Na-Chuan Jiang, Bin Tan, Xin-Yuan Liu
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652219

Abstract:
The first catalytic asymmetric aminotrifluoromethylation of alkenes by using Togni′s reagent (II) has been developed.
N. O. Mahmoodi, B. Sharifzadeh, M. Mamaghani, K. Tabatabaeian, S. Shoja
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652346

Abstract:
Title compounds (III) are prepared by TosOH-catalyzed reaction of aromatic aldehydes with (substituted) thiobarbituric acid.
Hermann Marius Feumo Feusso, Carine Mvot Akak, Michel Feussi Tala, Anatole Guy Blaise Azebaze, Nole Tsabang, Juliette Catherine Vardamides, Hartmut Laatsch
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652393

Qianwen Huang, Hanliang Zheng, Shuiyou Liu, Lichun Kong, Fang Luo,
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652204

Abstract:
A novel azidative cycloisomerization of homoallenyl amides (I) and (III) using TmsN3 as the azidation reagent and a hypervalent iodine reagent as the oxidant giving a series of azidomethyl-furans (II) and (IV), resp., is presented.
Arijit A. Adhikari,
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652236

Abstract:
Several C-3a-substituted pyrroloindolines are obtained by nucleophilic substitution reaction of appropriate pyrroloindolinol trichloroacetimidates utilizing anilines, alcohols, thiols, and carbon nucleophiles.
Maki Minakawa, Masataka Okubo, Motoi Kawatsura
Published: 6 December 2016
ChemInform, Volume 47; doi:10.1002/chin.201652075

Abstract:
The novel reaction conditions allow the direct mono-N-alkylation of primary aromatic amines.
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