𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A New Route for the Total Synthesis of 6,7-Dihydroeponemycin

✍ Scribed by Bibia Bennacer; Christian Rivalle; David S. Grierson


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
152 KB
Volume
2003
Category
Article
ISSN
1434-193X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Polyamide synthesis by ester aminolysis.
✍ F. Jouffret; P.-J. Madec 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 580 KB

A new route for nylon-6,6 synthesis has been studied. The process is grounded on the synthesis of an a-amino w-ester monoamide precursor (AME-6,6) easily available in reacting in the bulk hexamethylene diamine and dimethyl adipate a t a low temperature (T = 50°C) preferably in the presence of a phen

Stereoselective Routes for the Total Syn
✍ Gowravaram Sabitha; Nandyala M. Reddy; Muddala N. Prasad; Jhillu S. Yadav 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 German ⚖ 212 KB 👁 1 views

## Abstract magnified image A stereoselective total synthesis of (+)‐cryptocarya diacetate (**1**) was achieved by two different routes (__Schemes 2__ and __3__). The sequences involve LiAlH~4~/LiI reduction, ring‐closing metathesis, __Prins__ cyclization, __Wacker__ oxidation, and __Wittig__ olef