✦ LIBER ✦

Enantiospecific synthesis of α-amino ketones and β-amino alcohols from the reaction of N-(9-phenylfluoren-9-yl)-alanine oxazolidinone with organolithium reagents

✍ Scribed by M.Rita Paleo; F.Javier Sardina

Publisher: Elsevier Science
Year: 1996
Tongue: French
Weight: 221 KB
Volume: 37
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(96)00557-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Enantiospecific Syn

ChemInform Abstract: Enantiospecific Synthesis of N-(9-Phenylfluoren-9-yl)-α-amino Ketones.

✍ M. R. PALEO; M. I. CALAZA; F. J. SARDINA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

ChemInform Abstract: Enantiomerically Pu

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

✍ 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