𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Bisamides Derived from Azulene-1,3- and -5,7-dicarboxylic Acids as New Building Blocks for Anion Receptors

✍ Scribed by Tomasz Zieliński; Mariusz Kȩdziorek; Janusz Jurczak

Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
436 KB
Volume
14
Category
Article
ISSN
0947-6539

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enantiomeric 3,7-Dimethylocta-1,7-dienes
Enantiomeric 3,7-Dimethylocta-1,7-dienes as Useful Chiral Building Blocks. A New Access to Both Optical Antipodes of Natural (E)-3,7-Dimethyloct-2-ene-1,8-diol and (E)-3,7-Dimethyloct-2-ene-1,8-dicarboxylic Acid
✍ Wolfgang Giersch; Karl H. Schulte-Elte 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 German ⚖ 371 KB

## Abstract Ozonolysis of the easily available monoterpenoids (−)‐1 and (+)‐1 leads in high yield to the ketoaldehydes (−)‐4 and (+)‐4, which serve as convenient intermediates for efficient new routes to both optical antipodes of the naturally occurring octenediol (__E__)‐2 (__Monarch__ butterfly s

Total Synthesis of [3aS-(3aα,9aα,9bβ)]-3
Total Synthesis of [3aS-(3aα,9aα,9bβ)]-3a,4,5,9,9a,9b-Hexahydro-3a,6-dimethyl-1H-benz[e]indene-3,7(2H,8H)-dione and Derivatives, Building Blocks for the Synthesis of Glucocorticoids
✍ Daniewski, Andrzej Robert ;Piotrowska, Emilia ;Wojciechowska, Wanda 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 417 KB 👁 1 views

The natural and synthetic glucocorticoids are very important compounds commonly used as drugs against many diseases. Recently, we have reported the synthesis of some of the title compounds and their transformations into 6-methyl-5-androstene-3,11,17-trione 3-ethyleneacctal, a building block for the