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Deposition number 2166113 (for syn-7a) contains the supplementary crystallographic data for this paper. These data are provided free of charge by the joint Cambridge Crystallographic Data Centre and Fachinformationszentrum Karlsruhe Access Structures service http://www.ccdc.cam.ac.uk/structures.
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Cite the Following Article
A novel spirocyclic scaffold accessed via tandem Claisen rearrangement/intramolecular oxa-Michael addition
Anastasia Vepreva, Alexander Yanovich, Dmitry Dar’in, Grigory Kantin, Alexander Bunev and Mikhail Krasavin
Beilstein J. Org. Chem. 2022, 18, 1649–1655.
https://doi.org/10.3762/bjoc.18.177
How to Cite
Vepreva, A.; Yanovich, A.; Dar’in, D.; Kantin, G.; Bunev, A.; Krasavin, M. Beilstein J. Org. Chem. 2022, 18, 1649–1655. doi:10.3762/bjoc.18.177
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Scholarly Works
- Yanovich, A.; Vepreva, A.; Malkova, K.; Kantin, G.; Dar'in, D. Entry to new spiroheterocycles via tandem Rh(II)-catalyzed O-H insertion/base-promoted cyclization involving diazoarylidene succinimides. Beilstein journal of organic chemistry 2024, 20, 561–569. doi:10.3762/bjoc.20.48
