Journal article
Regiodivergent cyclobutanone cleavage: switching selectivity with different Lewis acids.
- Souillart L Laboratory of Asymmetric Catalysis and Synthesis, EPFL SB ISIC LCSA, BCH 4305, 1015 Lausanne (Switzerland), Fax: (+41) 21 693 97 00 http://isic.epfl.ch/lcsa.
- Cramer N
- 2014-12-06
Published in:
- Chemistry (Weinheim an der Bergstrasse, Germany). - 2015
English
The exploitation of strain release in small rings as driving force to enable complex transformations is a powerful synthetic tool. Among them, cyclobutanones are particularly versatile substrates that can be elaborated in a wide variety of structurally diverse building blocks. Herein, Lewis acid catalyzed rearrangement reactions are presented that provide selective access to two structurally distinct polycyclic scaffolds, that is, indenylacetic acid derivatives and benzoxabicyclo[3.2.1]octan-3-ones. The choice of the Lewis acid fully controls the reaction pathway and the regioselectivity of the cyclobutanone CC bond cleavage site.
- Language
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- English
- Open access status
- closed
- Identifiers
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- DOI 10.1002/chem.201406135
- PMID 25476844
- Persistent URL
- https://folia.unifr.ch/global/documents/190417
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