Reaction of 9-amino(phenylamino)methylene- and 9-α-aminobenzylidene-4-azafluorenes with some electrophilic reagents
✍ Scribed by A. V. Varlamov; A. N. Levov; V. V. Davydov; A. É. Aliev; A. P. Krapivko; G. V. Sheban; A. I. Skomorokhova; B. E. Zaitsev; N. S. Prostakoy
- Publisher
- Springer US
- Year
- 1995
- Tongue
- English
- Weight
- 532 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Enantiomerically Pure Highly Functionalized α-Amino Ketones from the Reaction of Chiral Cyclic N-(9-Phenylfluoren-9-yl) α-Amido Esters with Organolithium Reagents. -Treatment of the cyclic αand β-amino esters (II), (V), and (VIII) with organolithium compounds is found to give the corresponding keto
Reaction of ArSCl (Ar = phenyl or ortho-nitrophenyl) withendo-tricyclo[6.2.1.@~7]undeca-4,9diene-3,6dione (1) results in arm' addition across the norbcnnene carbon-carbon double bond with concomitant aromatization of the cyclohexenedione ring, thereby affording 4 (87%) and 5 (63%), respectively. Th