𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Approaches to the synthesis of cytochalasans. Part 10. Cuprates as reagents for the formation of CC bonds

✍ Scribed by Michael Matthes; Christoph Tamm

Publisher
John Wiley and Sons
Year
1991
Tongue
German
Weight
367 KB
Volume
74
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Approaches to the Synthesis of Cytochala
Approaches to the Synthesis of Cytochalasans. Part 2. Pyrrolinone derivatives as basic units
✍ Tibur Schmidlin; Christoph Tamm 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 German ⚖ 632 KB

## Abstract Several attempts to prepare 3‐acetyl‐5‐benzyl‐3‐pyrrolin‐2‐one (**7**) from phenylalanine are described. This goal was only reached formally, because compound **7** exists in the tautomeric form of (Z)‐5‐benzyl‐3‐(1′‐hydroxyethylidene)‐4‐pyrrolin‐2‐one (**17**) according to the spectral

Approaches to the synthesis of cytochala
Approaches to the synthesis of cytochalasans. Part 7. Synthesis of some building blocks for the construction of the macrocyclic moiety
✍ Daniel Wallach; Ivan G. Csendes; Peter E. Burckhardt; Tibur Schmidlin; Christoph 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 German ⚖ 563 KB

## Abstract The synthesis of ethyl (2__E__, 4__E__, 8__R__)‐8‐methyl‐10‐[(2__H__‐tetrahydropyran‐2‐yl)oxy]‐2,4‐decadienoate (**11**), methyl (2__E__, 8__R__)‐8‐methyl‐10‐[(2__H__‐tetrahydropyran‐2‐yl)oxy]‐2‐decenoate (**16**), synthons for the construction of the macrocyclic moieties of the cytocha

Approaches to the Synthesis of Cytochala
Approaches to the Synthesis of Cytochalasans. Part 3. Synthesis of a substituted tetrahydroisoindolinone moiety possessing the same relative configuration as proxiphomin
✍ Tibur Schmidlin; Werner Züurcher; Christoph Tamm 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 German ⚖ 769 KB

## Abstract The total synthesis of the tetrahydroisoindolinone moiety corresponding to proxiphomin (**1**) is described, bearing functional groups for the attachment of the macrocyclic ring. __Knoevenagel‐Cope__ condensation of racemic 2‐(benzyloxycarbonyl‐amino)‐3‐phenylpropanal (**2**) with methy