✦ LIBER ✦

Determination of the Absolute Configuration of Restricted 1,1'-Binaphthyls by Asymmetric Meerwein-Ponndorf-Verley Reduction 1

✍ Scribed by Mislow, Kurt; McGinn, Francis A.

Book ID: 126136112
Publisher: American Chemical Society
Year: 1958
Tongue: English
Weight: 411 KB
Volume: 80
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01555a036

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mechanism of the Meerwein-Ponndorf-Verle

Mechanism of the Meerwein-Ponndorf-Verley Reduction 1

✍ MOULTON, W. N.; ATTA, R. E. VAN; RUCH, R. R. 📂 Article 📅 1961 🏛 American Chemical Society 🌐 English ⚖ 339 KB

Catalysis of organic reactions by molecu

Catalysis of organic reactions by molecular sieve systems: 1. Meerwein-Ponndorf-Verley reductions

✍ Joseph Shabtai; R. Lazar; Ehud Biron 📂 Article 📅 1984 🏛 Elsevier Science ⚖ 620 KB

Conformation and Optical Rotation of Res

Conformation and Optical Rotation of Restricted Biphenyls. Configurational Correlation of Biaryls by Optical Displacement. The Absolute Configuration of Restricted 1,1'-Binaphthyls 1

✍ Fitts, Donald D.; Siegel, Maurice; Mislow, Kurt 📂 Article 📅 1958 🏛 American Chemical Society 🌐 English ⚖ 837 KB

Novel 1,3-diol monoethers by a triple ta

Novel 1,3-diol monoethers by a triple tandem aldolization/etherification/Meerwein–Ponndorf–Verley reduction of aliphatic aldehydes

✍ Nina Aremo; Tapio Hase 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 62 KB

A one-pot reaction of aliphatic aldehydes with TiCl 4 and Ti(O i Pr) 4 or isopropanol in CH 2 Cl 2 produces dimeric 3-hydroxyethers in moderate yield.

Asymmetric reduction and Meerwein-Ponndo

Asymmetric reduction and Meerwein-Ponndorf-Verley reaction of prochiral aromatic ketones in the presence of optically pure 1-aryl-2,2-dimethylpropane-1,3-diols

✍ Hu Xianming; Richard M. Kellogg 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 736 KB

## Abstract In THF solution, NaBH~4~ in the presence of (__S__)‐(‐)‐1‐(2‐chlorophenyl)‐2,2‐dimethylpropane‐1,3‐diol together with 2‐chlorobenzoic acid reduced propiophenone to 1‐ phenylpropan‐1‐ol in up to 40% enantiomeric excess (__ee__). Only 21% __ee__ was obtained without an added acid. (__R__)

The Asymmetric Meerwein–Schmidt–Ponndorf

The Asymmetric Meerwein–Schmidt–Ponndorf–Verley Reduction of Prochiral Ketones with iPrOH Catalyzed by Al Catalysts

✍ E. Joseph Campbell; Hongying Zhou; SonBinh T. Nguyen 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 72 KB 👁 1 views