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Nitrogen atom transfer to alkenes utilizing Chloramine-T as a nitrogen source

โœ Scribed by Takeya Ando; Satoshi Minakata; Ilhyong Ryu; Mitsuo Komatsu


Book ID
104258500
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
187 KB
Volume
39
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Nitrogen Atom Trans
โœ T. ANDO; S. MINAKATA; I. RYU; M. KOMATSU ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 2 views

Nitrogen Atom Transfer to Alkenes Utilizing Chloramine-T as a Nitrogen Source. -Readily available and inexpensive chloramine-T (II) is found to undergo a Cu(I)-catalyzed reaction with unfunctionalized alkenes in anhydrous acetonitrile providing N-tosyl aziridines in moderate yield. -

ChemInform Abstract: Iodine-Catalyzed Az
โœ T. ANDO; D. KANO; S. MINAKATA; I. RYU; M. KOMATSU ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 30 KB ๐Ÿ‘ 2 views

Iodine-Catalyzed Aziridination of Alkenes Using Chloramine-T as a Nitrogen Source. -The mechanism of the aziridination is not clear, but the participation of a iodine-Chloramine-T complex and an iodonium cation intermediate are suggested. Comparative reactions with p-substituted styrenes show that