𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Acenaphtho (1,2-c)thiophen und N-Methyl-acenaphtho (1,2-c)pyrrol

✍ Scribed by Jürgen Graefe; Manfred Mühlstädt


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
244 KB
Volume
9
Category
Article
ISSN
0044-2402

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Correlation of molecular orbital indices
✍ K. D. Bartle 📂 Article 📅 1973 🏛 John Wiley and Sons 🌐 English ⚖ 203 KB

## Abstract Nuclear magnetic resonance proton chemical shifts may be correlated with free valence, a representative reactivity index, for fluoranthene and two novel sulphur heterocyclic analogues, acenaphtho[1,2‐__b__]‐ and ‐[1,2‐__c__]thiophens. Such correlations arise fortuitously, however, and a

Palladium-Catalyzed Synthesis of 7,9-Dia
✍ Xiaopeng Chen; Jisong Jin; Prof. Yanguang Wang; Prof. Ping Lu 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 217 KB

Pyrrole is one of the most important heterocyclic compounds in nature. [1] Its derivatives are broadly found and developed as drugs in medicinal industry. [2] Meanwhile, they are closely related to optoelectronic material fields, such as pyrrole-based oligomer or organic field-effect transistors (OF

Dimethyl 6b,9a-dihydroxy­acenaphtho[1,2-
✍ Jimenez, Raphael P. ;Parvez, Masood ;Sutherland, Todd C. 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 175 KB

In the title compound, C 18 H 16 O 6 S, two hydroxy groups, having a syn regiochemistry, act as both hydrogen-bond donors and acceptors, resulting in the formation of an infinite molecular chain.