𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Application of MerCO as a Chiral Catalyst in Asymmetric Synthesis: Asymmetric Borane Reduction of Ketones.

✍ Scribed by Teng-Kuei Yang; Dong-Sheng Lee


Publisher
John Wiley and Sons
Year
2010
Weight
28 KB
Volume
30
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of a new C2-symmetric chiral c
✍ Yan Zhou; Wen-Hua Wang; Wei Dou; Xiao-Liang Tang; Wei-Sheng Liu 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 120 KB 👁 1 views

## Abstract A new __C__~2~‐symmetric chiral catalyst 3,5‐bis[(2__S__)‐(hydroxy‐diphenylmethyl)‐ pyrrolidin‐1‐ylmethyl]‐1,3,4‐oxadiazole was successfully synthesized by the reaction of 2,5‐dichloromethyl‐1,3,4‐oxadiazole with (__S__)‐α,α‐diphenyl‐2‐pyrrolidinemethanol, and applied to the catalytic a

ChemInform Abstract: A Novel Phosphinami
✍ M. P. GAMBLE; A. R. C. SMITH; M. WILLS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

A Novel Phosphinamide Catalyst for the Asymmetric Reduction of Ketones by Borane. -The novel phosphinamide ("cat.") is a readily available, robust, versatile and recoverable reagent for the catalytic asymmetric reduction of ketones by borane. -(GAMBLE, M.

Synthesis of N-squaramidoacids and their
✍ Ji Zhang; Lei-Lei Li; Hai-Hua Zou; Jun-Jun Chen; Kai-Bei Yu; Ru-Gang Xie 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 427 KB

## Abstract A series of novel __N__‐squaramidoacid ligands were prepared conveniently. Without converting to corresponding amino alcohols, these ligands could be used in asymmetric borane reduction of prochiral aromatic ketones to give secondary alcohols in good to excellent enantiomeric excesses.