Year: 2026
Type: article
Abstract: A small panel of non-racemic 1-(α-methylbenzylamino)cyclobutanes bearing one-carbon functional groups at C1 of the cyclobutane ring was targeted. Successful synthetic procedures were established to access the target molecules, with the exception of the C1-formyl derivative whose electrophilicity was incompatible with the free secondary amine. When a C1 nucleofugal group was generated, cyclization occurred leading to a novel spiroaziridine derivative.
Source: Tetrahedron Letters
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $3,610
Award: G9000359726
OpenAlex ID: W7213223774
