Synthesis and modelling of novel rigid rods derived from a simple pentacyclic bis-norbornene [1]
✍ Scribed by Davor Margetic; Martin R. Johnston; Edward R.T. Tiekink; Ronald N. Warrener
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 230 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
New rigid rods with 4~, 6c, 10~, 12~, and 16~ bond separations have been prepared from the pentacyclic diene 3 using ACE (alkene plus cyclobutene epoxide) and s-tetrazine coupling techniques and their shapes evaluated using AM1 calculations. The X-ray structure of the 6~-rod 5 is reported.
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## Abstract magnified image 3‐Imino‐2‐amino‐isatines were obtained by a one‐pot reaction of an excess of aniline (or its derivatives) with 1,2‐bis(dimethylamino)‐1,2‐dichloro‐ethene (prepared __in situ__ from DMF). Subsequent hydrolysis yielded the corresponding isatine derivatives in reasonable t