✦ LIBER ✦

Asymmetric organolithium additions to imines

✍ Scribed by Kiyoshi Tomioka; Isao Inoue; Mitsuru Shindo; Kenji Koga

Publisher: Elsevier Science
Year: 1990
Tongue: French
Weight: 191 KB
Volume: 31
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)97146-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric addition of organolithium rea

Asymmetric addition of organolithium reagents to imines favouring (S)-amines

✍ Catrin A. Jones; Iwan G. Jones; Michael North; Colin R. Pool 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 243 KB

ChemInform Abstract: Synthesis and Appli

ChemInform Abstract: Synthesis and Application of Ligands for the Asymmetric Addition of Organolithium Reagents to Imines.

✍ C. A. JONES; I. G. JONES; M. MULLA; M. NORTH; L. SARTORI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

ChemInform Abstract: Studies on the Scop

ChemInform Abstract: Studies on the Scope and Applications of the Catalyzed Asymmetric Addition of Organolithium Reagents to Imines.

✍ C. A. JONES; M. NORTH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

ChemInform Abstract: A Facile Asymmetric

ChemInform Abstract: A Facile Asymmetric Synthesis of 1-Substituted Tetrahydroisoquinoline Based on a Chiral Ligand-Mediated Addition of Organolithium to Imine.

✍ Daisuke Taniyama; Masayoshi Hasegawa; Kiyoshi Tomioka 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

Catalytic asymmetric addition of organol

Catalytic asymmetric addition of organolithiums to aldimines

✍ Kiyoshi Tomioka; Isao Inoue; Mitsuru Shindo; Kenji Koga 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 261 KB

Organolithium additions to allylic alcoh

Organolithium additions to allylic alcohols

✍ J.K. Crandall; A.C. Clark 📂 Article 📅 1969 🏛 Elsevier Science 🌐 French ⚖ 181 KB

Simple organolithium reagents do not generally add to nonconjugated olefins'; although instances of such reactions have been reported in which particularly strained olefins were used,lj2 a substantially more stable organolithium species was formed,lJ4 or the reaction was intramolecular in nature'.