𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A new strategy for the stereospecific syntheses of C-furanosides

✍ Scribed by Bing-Hui Yang; Ji-Qing Jiang; Xi-Lin Huang; Hou-Ming Wu

Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
544 KB
Volume
15
Category
Article
ISSN
0256-7660

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Unified Strategy for the Asymmetric To
A Unified Strategy for the Asymmetric Total Syntheses of Diversonol and Lachnone C
✍ Dipl.-Chem. Manuel C. Bröhmer; Dr. Emmanuel Bourcet; Dr. Martin Nieger; Prof. Dr 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 320 KB 👁 2 views

## Abstract A unified synthetic strategy for the asymmetric syntheses of the natural products diversonol and lachnone C was developed by using the domino vinylogous aldol–oxa‐Michael reaction as the enantioselective key step. Further transformations include dihydroxylation, lactol‐opening by a Witt

Aziridines as templates: A general strat
Aziridines as templates: A general strategy for the stereospecific synthesis of 2-azetidinones
✍ S. D. Sharma; Seema Kanwar; Shivani Rajpoot 📂 Article 📅 2006 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 147 KB

## Abstract magnified image Various routes to a variety of azridine‐2‐carboxylates have been described and the stereochemistry of these compounds has been determined by spectroscopic methods. Further, greater diversity of β‐lactams __via__ ring expansion of these azridines‐2‐carboxylates were obta