Light-enabled scalable synthesis of bicyclo[1.1.1]pentane halides and their functionalizations-Reference-Cited by-同舟云学术

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Light-enabled scalable synthesis of bicyclo[1.1.1]pentane halides and their functionalizations

Published:2024-09-05 Issue: Volume: Page:
ISSN:2731-0582
Container-title:Nature Synthesis
language:en
Short-container-title:Nat. Synth

Author:

Ripenko Vasyl^ORCID,Sham Vadym^ORCID,Levchenko Vitalina^ORCID,Holovchuk Serhii,Vysochyn Daniil,Klymov Ivan,Kyslyi Dmytro,Veselovych Stanislav,Zhersh Serhii^ORCID,Dmytriv Yurii,Tolmachev Andrey,Sadkova Iryna,Pishel Irina^ORCID,Horbatok Kateryna,Kosach Viktoria^ORCID,Nikandrova Yelyzaveta,Mykhailiuk Pavel K.^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s44160-024-00637-y.pdf

Reference110 articles.

1. Taylor, R. D., MacCoss, M. & Lawson, A. D. G. Rings in drugs. J. Med. Chem. 57, 5845–5859 (2014).

2. Shearer, J., Castro, J. L., Lawson, A. D. G., MacCoss, M. & Taylor, R. D. Rings in clinical trials and drugs: present and future. J. Med. Chem. 65, 8699–8712 (2022).

3. Chen, Y., Rosenkranz, C., Hirte, S. & Kirchmair, J. Ring systems in natural products: structural diversity, physicochemical properties, and coverage by synthetic compounds. Nat. Prod. Rep. 39, 1544–1556 (2022).

4. Stepan, A. F. et al. Application of the bicyclo[1.1.1]pentane motif as a nonclassical phenyl ring bioisostere in the design of a potent and orally active γ-secretase inhibitor. J. Med. Chem. 55, 3414–3424 (2012).

5. Mykhailiuk, P. K. Saturated bioisosteres of benzene: where to go next? Org. Biomol. Chem. 17, 2839–2849 (2019).

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