𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Sterically Hindered Cyclic Diynes − Syntheses and Structures

✍ Scribed by Carsten Schaefer; Rolf Gleiter; Frank Rominger


Book ID
102176762
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
272 KB
Volume
2003
Category
Article
ISSN
1434-193X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The synthesis of three 14‐membered ring systems 8a8c with the 1,3,8,10‐tetraoxa‐2,9‐disilacyclotetradeca‐5,12‐diyne skeleton is described. In all three ring systems the α‐positions are substituted with gem‐dimethyl and/or gem‐diphenyl groups. Structural investigations on 8a and 8c reveal a chair like conformation of the central ring with parallel alkyne units. For 8b the voluminous phenyl groups cause a twist‐chair and a twist‐boat conformation. Columnar structures were encountered for 8a in the solid state. Reactions with octacarbonyldicobalt yield for 8a mono‐ and biscomplexation (12, 13). For 8b only the mono complexation product 14 was isolated. For 8c the bis(hexacarbonyldicobalt) complex 15 was obtained. X‐ray investigations revealed columnar structures in the solid state for 12, 13, and 15. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)


📜 SIMILAR VOLUMES


Cover Picture: Sterically Hindered Cycli
✍ Carsten Schaefer; Rolf Gleiter; Frank Rominger 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 69 KB

## Abstract **The cover picture shows** on the left‐hand side a sterically hindered cyclic diyne and its synthesis. The packing of the molecules in the crystal is depicted in the center. Within the crystal weak intermolecular interactions were found that are illustrated on the right‐hand side. For

Thiocarbonyl ylides and electrophilic az
✍ Rolf Huisgen; Xingya Li; Grzegorz Mloston; Rudolf Knorr; Helmut Huber; David S S 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 889 KB

The cycloadduct 5, prepared from adamantanethione S-methylide with dimethyl azodicarboxylate, exists in solution in two conformations P and Q (70:30 in CDCI3), which are selm~ted by a barrier of AG~ 18.3 + 0.6 kcal mol-I; according to NMR spectra, both forms are chiral. Steric hindrance to 3'N-CO2CH