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Enantiomerically Pure Highly Functionalized α-Amino Ketones from the Reaction of Chiral Cyclic N -(9-Phenylfluoren-9-yl) α-Amido Esters with Organolithium Reagents

✍ Scribed by Fernández-Megía, Eduardo; Iglesias-Pintos, José M.; Sardina, F. Javier


Book ID
126159517
Publisher
American Chemical Society
Year
1997
Tongue
English
Weight
423 KB
Volume
62
Category
Article
ISSN
0022-3263

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ChemInform Abstract: Enantiomerically Pu
✍ E. FERNANDEZ-MEGIA; J. M. IGLESIAS-PINTOS; F. J. SARDINA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

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