𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Simple New Method for the Synthesis of 2-Deoxy-aldehydo-hexoses

✍ Scribed by Dr. Wilhelm V. Dahlhoff; Prof. Dr. Roland Köster

Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
228 KB
Volume
19
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ortho-Thioquinones, New Acceptors for th
ortho-Thioquinones, New Acceptors for the Stereoselective Synthesis of Aryl 2-Deoxy-O-Glycosides
✍ Giuseppe Capozzi; Chiara Falciani; Stefano Menichetti; Cristina Nativi; Barbara 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 187 KB 👁 1 views

a-Hydroxynaphthylthiophthalimide (1) is a suitable precursor of the reactive ortho-thioquinone 2, which can be generated in situ and trapped by glycals. The reaction is an inverse electron-demand [42] cycloaddition that occurs in a totally regioselective and highly stereoselective way. A series of d

New Method for the Synthesis of N-Vinyla
New Method for the Synthesis of N-Vinylamides.
✍ Priv.-Doz. Dr. Günter Schmitt; Dr. Wolfgang Ebertz 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 205 KB 👁 2 views

## Abstract The complete manuscript of this communication appears in: __Angew. Chem. Suppl. 1982__, 1440. DOI:10.1002/anie.198214400

A new method for the synthesis of thieno
A new method for the synthesis of thieno[2,3-c]pyrazoles
✍ Zhongwen Wang; Zhengming Li; Jun Ren; Hansong Chen 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 124 KB 👁 2 views

A new method has been found for the synthesis of pyrazoleacetate esters from pyrazolaldehyde. By a new tandem reaction, in which methyl 4pyrazoleacetate was reacted with carbon disulfide and iodomethane, thieno [2,3-c]pyrazole was synthesized. This was an easy method for the synthesis of this type o

A Thermostable Aldolase for the Synthesi
A Thermostable Aldolase for the Synthesis of 3-Deoxy-2-ulosonic Acids
✍ Henry J. Lamble; Sylvain F. Royer; David W. Hough; Michael J. Danson; Garry L. T 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB 👁 1 views

## Abstract A stereochemically promiscuous 2‐keto‐3‐deoxygluconate aldolase has been used as an efficient biocatalyst to catalyse the aldol reaction of pyruvate with C~3~‐ and C~4~‐aldoses to afford __syn__‐ and __anti__‐3‐deoxy‐2‐ulosonic acids in poor to good __de__. A continuous flow bioreactor