𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Enantioselective reduction of diethyl 2-oxoalkylphosphonates by baker's yeast

✍ Scribed by Ewa Żymańczyk-Duda; Barbara Lejczak; Pawel Kafarski; Jean Grimaud; Peter Fischer


Publisher
Elsevier Science
Year
1995
Tongue
French
Weight
353 KB
Volume
51
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Enantioselective reduction of 2-keto-3-h
✍ Cheng-ye Yuan; Ke Wang; Zu-yi Li 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB 👁 1 views

## Abstract Bioreduction of 3‐substituted‐2‐oxoal‐kanephosphonates by baker's yeast afforded 3‐substituted‐2‐hydroxy‐alkanephosphonates in moderate to good yields and ee value. These compounds could serve as useful chirons for the stereoselective synthesis of phosphorus analogs of biologically acti

Baker′s Yeast-Mediated Enantioselective
✍ Feng Li; Jingnan Cui; Xuhong Qian; Weimin Ren; Xingyong Wang 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 16 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Enantioselective reduction of dialkyl 4-
✍ Chengye Yuan; Ke Wang; Jinfeng Li; Zuyi Li 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 120 KB 👁 1 views

## Abstract Dialkyl 4‐(dialkoxyphosphoryl)‐3‐oxobutanoates (**__1__**), upon yeast‐mediated bioreduction, afforded chiral dialkyl 4‐(dialkoxyphosphoryl)‐3‐hydroxybutanoates (**__2__**) in moderate to good yields and ee values. Significant improvement was reported for the preparation of dialkyl 4‐(d