Conformational Lability of Bispidine as a Route to New Polycyclic Compounds Full article
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Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263 |
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| Output data | Year: 2026, Volume: 91, Number: 43, Pages: 14341–14345 Pages count : DOI: 10.1021/acs.joc.6c01744 | ||
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Abstract:
In this study, novel tricyclic compounds based on bispidine were prepared via a Michael addition−Henry domino reaction.
This reaction sequence proceeds under mild conditions with high diastereoselectivity. Postsynthetic transformation pathways for
the resulting nitro alcohols were demonstrated, leading to tricyclic amino alcohols of various structures.
Cite:
Medved'ko A.V.
, Vatsadze S.Z.
Conformational Lability of Bispidine as a Route to New Polycyclic Compounds
Journal of Organic Chemistry. 2026. V.91. N43. P.14341–14345. DOI: 10.1021/acs.joc.6c01744 WOS Scopus OpenAlex
Conformational Lability of Bispidine as a Route to New Polycyclic Compounds
Journal of Organic Chemistry. 2026. V.91. N43. P.14341–14345. DOI: 10.1021/acs.joc.6c01744 WOS Scopus OpenAlex
Dates:
| Submitted: | Jul 20, 2026 |
| Accepted: | Oct 13, 2026 |
| Published print: | Oct 20, 2026 |
| Published online: | Oct 30, 2026 |
Identifiers:
| ≡ Web of science: | WOS:001907901000001 |
| ≡ Scopus: | 2-s2.0-105055012290 |
| ≡ OpenAlex: | W7223064614 |