𝔖 Bobbio Scriptorium
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Oligonucleotide Synthesis with Trichloroacetonitrile

✍ Scribed by Prof. Dr. F. Cramer; Dr. H. J. Baldauf; cand. ing. H. Küntzel


Book ID
101543975
Publisher
John Wiley and Sons
Year
1962
Tongue
English
Weight
126 KB
Volume
1
Category
Article
ISSN
0044-8249

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✦ Synopsis


  1. to l-azacyclohepta-4,7-diene-2-one (IV) and prototropic rearrangement [3]. Attempts to convert (V) into the hitherto unknown azepine, or its derivatives, are in progress. For the liquid isomer (VI), the structure of a 2-vinylcyclopropyl isocyanate was proven by IR spectral and nuclear magnetic resonance data. Since (V) is to be considered as the rearrangement product of (III), (VI) must have the trans configuration. trans-2-Vinylcyclopropyl isocyanate has remarkable thermal stability. Even when heated for 2 hours to 200 "C., it is only slightly polymerized.

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