𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A new route to 2,2′,3,3′-tetrasubstituted binaphthyls

✍ Scribed by Michael Widhalm; Christian Aichinger; Kurt Mereiter


Book ID
108285471
Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
656 KB
Volume
50
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A new route to 2′,3′-dideoxycytidine
✍ Motawia, Mohammed S. ;Pedersen, Erik B. 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 384 KB

## Abstract 2‐Deoxy‐D‐ribose (1) was converted into its methyl glycofuranoside 2, which was treated with 4‐biphenylcarbonyl chloride to give a separable mixture of 3 (26%) and 4 (40%). Compounds 3 and 4 were deoxygenated by Barton deoxygenation to give the corresponding 2,3‐dideoxyribose derivative

A New Approach to the Synthesis of 1,2,3
✍ S. A. Vizer; E. H. Dedeshko; K. B. Yerzhanov; V. M. Dembitsky 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 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.

A new approach to the synthesis of 1,2,3
✍ S. A. Vizer; E. H. Dedeshko; K. B. Yerzhanov; V. M. Dembitsky 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 129 KB 👁 1 views

## Abstract 2‐Propargyl‐1,3‐dicarbonyl derivatives, namely the corresponding cumulenes and diethoxyphosphoryloxy containing substances in the reactions with primary amines, are converted into the corresponding 1,2,3,5‐tetrasubstituted pyrroles. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:220–