✦ LIBER ✦

Diastereoselective synthesis of a resolved secondary arsine complex: asymmetric synthesis of (R-(−)589-ethylmethylphenylarsine

✍ Scribed by Geoffrey Salem; S.Bruce Wild

Book ID: 107811518
Publisher: Elsevier Science
Year: 1989
Tongue: English
Weight: 691 KB
Volume: 370
Category: Article
ISSN: 0022-328X
DOI: 10.1016/0022-328x(89)87272-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Diastereoselective synthesis of a “chira

Diastereoselective synthesis of a “chiral-at-Ru” secondary phosphine complex

✍ Gregory L. Gibson; Krista M.E. Morrow; Robert McDonald; Lisa Rosenberg 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 613 KB

Diastereoselective catalytic asymmetric

Diastereoselective catalytic asymmetric nitroaldol reaction utilizing rare earth-Li-(R)-BINOL complex. A highly efficient synthesis of norstatine

✍ Hiroaki Sasai; Won-Sup Kim; Takeyuki Suzuki; Masakatsu Shibasaki; Masaru Mitsuda 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 321 KB

Asymmetric synthesis via acetal template

Asymmetric synthesis via acetal templates. 12. Highly diastereoselective coupling reactions with a ketene acetal. An efficient, asymmetric synthesis of R-(+)-α-lipoic acid

✍ John D. Elliott; John Steele; William S. Johnson 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 285 KB

Diastereoselective [4 + 2] type cycloadd

Diastereoselective [4 + 2] type cycloaddition of 1-azatriene iron-tricarbonyl complex: Asymmetric synthesis of a piperidien alkaloid

✍ Yoshiji Takemoto; Shigeo Ueda; Jun Takeuchi; Takahisa Nakamoto; Chuzo Iwata 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 289 KB

Asymmetric hydrogenation of enol phosphi

Asymmetric hydrogenation of enol phosphinates catalyzed by a chiral ferrocenylphosphine-rhodium complex. Asymmetric synthesis of optically active secondary alkyl alcohols

✍ Tarnio Hayashi; Koichi Kanehira; Makoto Kumada 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 273 KB

First asymmetric synthesis of (2R, 3R)-3

First asymmetric synthesis of (2R, 3R)-3-amino-1-benzyl-2-methyl-pyrrolidine via a highly diastereoselective reductive alkylation

✍ Pei Qiang Huang; Si Li Wang; Hong Zheng; Xiang Su Fei 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 117 KB

The first asymmetric synthesis of (2R, 3R)-3-amino-l-benzyl-2-methylpyrrolidine, the parent diamine of antipsychotic agent, emonapride, from (S)-malic acid was achieved via a highly diastereroselective reductive alkylation.