✦ LIBER ✦

Asymmetric Catalytic Synthesis of Enantiopure N -Protected 1,2-Amino Alcohols

✍ Scribed by Bartoli, Giuseppe; Bosco, Marcella; Carlone, Armando; Locatelli, Manuela; Melchiorre, Paolo; Sambri, Letizia

Book ID: 119992493
Publisher: American Chemical Society
Year: 2004
Tongue: English
Weight: 58 KB
Volume: 6
Category: Article
ISSN: 1523-7060
DOI: 10.1021/ol048322l

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric Catalytic Synthesis of Enanti

Asymmetric Catalytic Synthesis of Enantiopure N-Protected 1,2-Amino Alcohols.

✍ Giuseppe Bartoli; Marcella Bosco; Armando Carlone; Manuela Locatelli; Paolo Melc 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 39 KB

Practical Synthesis of Enantiopure Cycli

Practical Synthesis of Enantiopure Cyclic 1,2-Amino Alcohols via Catalytic Asymmetric Ring Opening of Meso Epoxides

✍ Schaus, Scott E.; Larrow, Jay F.; Jacobsen, Eric N. 📂 Article 📅 1997 🏛 American Chemical Society 🌐 English ⚖ 131 KB

ChemInform Abstract: Practical Synthesis

ChemInform Abstract: Practical Synthesis of Enantiopure Cyclic 1,2-Amino Alcohols via Catalytic Asymmetric Ring Opening of meso Epoxides.

✍ S. E. SCHAUS; J. F. LARROW; E. N. JACOBSEN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Asymmetric Synthesis of Protected 1,2-Am

Asymmetric Synthesis of Protected 1,2-Amino Alcohols Using tert -Butanesulfinyl Aldimines and Ketimines

✍ Tang, Tony P.; Volkman, Steven K.; Ellman, Jonathan A. 📂 Article 📅 2001 🏛 American Chemical Society 🌐 English ⚖ 108 KB

ChemInform Abstract: Asymmetric Synthesi

ChemInform Abstract: Asymmetric Synthesis of Protected 1,2-Amino Alcohols Using tert-Butanesulfinyl Aldimines and Ketimines.

✍ Tony P. Tang; Steven K. Volkman; Jonathan A. Ellman 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

Asymmetric synthesis of 2-amino-1-arylet

Asymmetric synthesis of 2-amino-1-arylethanols by catalytic asymmetric hydrogenation

✍ Tamio Hayashi; Akifumi Katsumura; Mitsuo Konishi; Makoto Kumada 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 249 KB

It is well documented that the d-and l-isomers of 2-amino-l-arylethanols such as epinephrine show a different biological and pharmacological activity,' and the optical isomers have been obtained through the resolution of the racemate' or from optically active precursors by chemical transformation.2