Construction of tetralin and chromane cores by the Lewis acid promoted ring-opening cyclization of cyclopropyl methanesulfonates

[Display omitted] Rearrangement of cyclopropyl methanesulfonates to allylic carbocations was employed for the construction of tetralin and chromate bicyclic cores. We found that this transformation proceeds efficiently and rapidly at room temperature in the presence of dimethylaluminium triflate ser...

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Bibliographic Details

Published in:	Tetrahedron letters Vol. 104; p. 154025
Main Authors:	Novikau, Ilya, Leushukou, Andrei, Tsiuryn, Mikita, Hurski, Alaksiej
Format:	Journal Article
Language:	English
Published:	Elsevier Ltd 17-08-2022
Subjects:	Chromanes Cyclopropanols Cyclopropyl-allyl rearragemet Lewis acid Tetralines Lewis acid Cyclopropyl-allyl rearragemet Tetralines Cyclopropanols Chromanes
Online Access:	Get full text
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