ChemInform Abstract: Intramolecular SN2 Reaction at α-Carbon of Trifluoromethyl Group: Preparation of Optically Active 2-Trifluoromethylaziridine.

ChemInform Abstract: General Syntheses o

ChemInform Abstract: General Syntheses of Optically Active α-Trifluoromethylated Amines via Ring-Opening Reactions of N-Benzyl-2-trifluoromethylaziridine.

✍ Toshimasa Katagiri; Mikihiro Takahashi; Yasuyuki Fujiwara; Hideki Ihara; Kenji U 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 41 KB

ChemInform Abstract: Preparation of Opti

ChemInform Abstract: Preparation of Optically Pure α-Trifluoromethyl-α-amino Acids from N-Tosyl-2-trifluoromethyl-2-alkyloxycarbonyl Aziridine.

✍ Toshimasa Katagiri; Yousuke Katayama; Mayuko Taeda; Takanori Ohshima; Naomi Iguc 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 47 KB 👁 1 views

ChemInform Abstract: Catalytic Activatio

ChemInform Abstract: Catalytic Activation of the Leaving Group in the SN2 Reaction.

✍ Hirofumi Yamamoto; Ghanshyam Pandey; Yumiko Asai; Mayo Nakano; Atsushi Kinoshita 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 46 KB 👁 1 views

ChemInform Abstract: The Preparation of

ChemInform Abstract: The Preparation of Optically Active α-Amino 4H-[1,2,4]Oxadiazol-5-ones from Optically Active α-Amino Acids.

✍ John E. Mangette; Matthew R. Johnson; Van-Duc Le; Rajesh A. Shenoy; Howard Roark 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 56 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Microbial Oxidation

ChemInform Abstract: Microbial Oxidation of 1,2-Diols Bearing a Substituent with an Oxyfunctional Group: Preparation of Optically Active 1,2-Diols and α-Hydroxy Ketones.

✍ Kazutsugu Matsumoto; Key Hashimoto; Mari Sakuragi; Ayumi Kusunoki; Masaki Nogawa 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 views

ChemInform Abstract: Phenylation Reactio

ChemInform Abstract: Phenylation Reaction of α-Acylnitromethanes to Give 1,2-Diketone Monooximes: Involvement of Carbon Electrophile at the Position α to the Nitro Group.

✍ Mikihiro Takamoto; Hiroaki Kurouchi; Yuko Otani; Tomohiko Ohwada 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v