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Two Novel Thermal Biradical Cyclizations of Enyne-Ketenimines: Theory, Experiment, and Synthetic Potential

✍ Scribed by Michael Schmittel; Jens-Peter Steffen; Miguel Á. Wencesla Ángel; Bernd Engels; Christian Lennartz; Michael Hanrath


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
110 KB
Volume
37
Category
Article
ISSN
0044-8249

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✦ Synopsis


Both benzocarbazoles and quinolines can be synthesized from enyne ketenimines 1 generated in situ via biradical intermediates (see reaction below). Which of the heterocyclic ring systems is formed depends on the choice of the substituent R at the alkyne terminus.


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